international classification of disease, 10th revision ...diagnostic codes related to family infant...

Diagnostic Codes Related to Family Infant Toddler (FIT) Program

1 | Page ICD-10 Codes Revised October 2015

International Classification of Disease, 10th Revision (ICD-10)


Revised October 2015

The following relevant diagnosis codes under the four Family Infant Toddler Program eligibility categories are taken

directly from the International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM).



Introduction:

The following is a guide for Family Infant Toddler (FIT) Program providers to determine the whether the child’s medical diagnosis meets

eligibility under the “Established Condition” or “Medical / Biological Risk”, in accordance with the Requirements for Family Infant Toddler

Early Intervention Services (NMAC 7.30.8). This guide is also to be used to determine the diagnostic billing codes (ICD-10 International

Classification of Diseases) to be entered into FIT-KIDS (Key Information Data System) for any the FIT eligibility criteria.

This guide is categorized by four main categories of Developmental Delay, Established Condition, Medical/Biological Risk Condition, and

Environmental Risk Factors. All codes have been converted from the ICD-9 to ICD-10 mapping.

The categories of Established Condition, and Medical/Biological Risk Condition have their own subcategories of the following: Genetic

Disorders; Mental/Psychosocial Disorders (DC: 0-3 diagnosis are indicated in bold); Neurologic/Musculoskeletal; Perinatal Factors;

Physical Impairments; and Sensory Abnormalities.

Reminder: Eligibility determination in the categories of Medical/Biological Risk Condition and Established Condition shall be made by a

license Medical Practitioner.

The category of Environmental Risk Factors have subcategories of the following: Other personal history presenting hazards to health;

Family history of certain chronic disabling diseases; family history of certain other specific conditions; family history of other conditions;

health supervision of a child; housing, household, and economic circumstances; other family circumstances; and other psychosocial

circumstances.

Reminder: Eligibility determination in the category of Environmental Risk Factors shall be made using the Environmental Risk Assessment

(ERA) tool approved by the FIT program.

Any questions regarding conditions not on this guide must be directed to your FIT Manager who will work with a New Mexico

Department of Health Medical Director/Physician to determine whether a proposed condition will be recognized. Reminder that there are

100,000 more codes in the ICD-10 conversion which makes the mapping process take longer.

Family Infant Toddler (FIT) Providers may keep this document electronically and in print. Note, that the electronic version has the option to

find sections by clicking the table of contents (hyperlinks), diagnosis and ICD-10 Codes can also be found by clicking CTRL+F.

Note: for billing purposes through FIT-KIDS all codes that are not listed on the drop-down list may be entered in the Field/Box of “Other

ICD-10 Code”.

Please contact your FIT Program Manager if you have any questions.



Table of Contents

DEVELOPMENTAL DELAY ....................................................................................................................................................................................................................................................................... 5

ESTABLISHED CONDITION: GENETIC DISORDERS ....................................................................................................................................................................................................................... 6

ESTABLISHED CONDITION: NEUROLOGIC/MUSCULOSKELETAL ......................................................................................................................................................................................... 10

ESTABLISHED CONDITION: PERINATAL FACTORS .................................................................................................................................................................................................................... 12

ESTABLISHED CONDITION: PHYSICAL IMPAIRMENTS ............................................................................................................................................................................................................. 13

ESTABLISHED CONDITION: SENSORY ABNORMALITIES ......................................................................................................................................................................................................... 14

MEDICAL/BIOLOGICAL RISK CONDITION: GENETIC DISORDERS........................................................................................................................................................................................ 17

MEDICAL/BIOLOGICAL RISK CONDITION: MENTAL/PSYCHOSOCIAL DISORDERS ....................................................................................................................................................... 22

MEDICAL/BIOLOGICAL RISK CONDITION: PERINATAL FACTORS ....................................................................................................................................................................................... 29

MEDICAL/BIOLOGICAL RISK CONDITION: PERINATAL FACTORS (CONTINUED) .......................................................................................................................................................... 30

MEDICAL/BIOLOGICAL RISK CONDITION: PHYSICAL IMPAIRMENTS ................................................................................................................................................................................ 31

MEDICAL/BIOLOGICAL RISK CONDITION: SENSORY ABNORMALITIES ............................................................................................................................................................................ 32

MEDICAL/BIOLOGICAL RISK CONDITION: SENSORY ABNORMALITIES (CONTINUED) ............................................................................................................................................... 33

ENVIRONMENTAL RISK FACTORS: PERSONAL HISTORY PRESENTING HAZARD TO HEALTH ................................................................................................................................. 34



ENVIRONMENTAL RISK FACTORS: FAMILY HISTORY OF CERTAIN CHRONIC DISABLING DISEASES ................................................................................................................... 34

ENVIRONMENTAL RISK FACTORS: FAMILY HISTORY OF OTHER CONDITIONS ............................................................................................................................................................. 35

ENVIRONMENTAL RISK FACTORS: HEALTH SUPERVISION OF INFANT OR CHILD ....................................................................................................................................................... 35

ENVIRONMENTAL RISK FACTORS: HOUSING, HOUSEHOLD, AND ECONOMIC CIRCUMSTANCES ......................................................................................................................... 36

ENVIRONMENTAL RISK FACTORS: OTHER FAMILY CIRCUMSTANCES .............................................................................................................................................................................. 36

ENVIRONMENTAL RISK FACTORS: OTHER FAMILY CIRCUMSTANCES (CONTINUED) ................................................................................................................................................. 37

ENVIRONMENTAL RISK FACTORS: OTHER PSYCHOSOCIAL CIRCUMSTANCES.............................................................................................................................................................. 37



Developmental Delay

A delay of 25% or more, after correction for prematurity, in one or more of the following areas of development: cognitive; communication; physical/motor; social or emotional; or adaptive of the following: (NMAC 7.30.8.10.9 Requirements for Family Infant Toddler Early Intervention Services.)

Condition Type ICD-10 Code Condition/Diagnosis

Development F70 Mild Intellectual Disabilities

Development F71 Moderate Intellectual Disabilities

Development F72 Severe Intellectual Disabilities

Development F73 Profound Intellectual Disabilities

Development F79 Unspecified Intellectual Disabilities

Development F80.1 Expressive Language Disorder

Development F80.2 Mixed Receptive-Expressive Language Disorder

Development F80.81 Childhood Onset Fluency Disorder

Development F80.89 Other developmental disorders of speech and language

Development F82 Specific Developmental Disorder of Motor Functions (Mixed Development Disorder)

Development F84.0 Autistic Disorder (DC 0-3 R: 710 Multisystem Development Disorder)

Development F84.9 Pervasive Development Disorder (PDD), Unspecified

Development F88 Other disorders of psychological development Mixed Development Disorder

Development F89 Other disorders of psychological development Other Specified Delays in Development



ESTABLISHED CONDITION: Genetic Disorders

A diagnosed physical, mental, or neurobiological condition that has a high probability of resulting in developmental delay. The established condition shall be diagnosed by a health care provider and documentation shall be kept on file. Established conditions include the following: (NMAC 7.30.8.10.9 Requirements for Family Infant Toddler Early Intervention Services.)


Genetic Disorders A81.1 Subacute Sclerosing Panencephalitis

Genetic Disorders D33.2 Benign Neoplasm of Brain, Unspecified

Genetic Disorders E70.20 Disorder of tyrosine metabolism, unspecified

Genetic Disorders E70.21 Tyrosinemia, Type I (Tyrosinosis) and Type II (Richner-Hanhart Syndrome)

Genetic Disorders E70.29 Disorder of tyrosine metabolism, unspecified

Genetic Disorders E70.8 Other disorders of aromatic amino-acid metabolism (Waardenburg's Syndrome, Type I)

Genetic Disorders E70.9 Disorder of aromatic amino-acid metabolism, unspecified

Genetic Disorders E72.03 Lowe's Syndrome or (Oculocerebrorenal Syndrome)

Genetic Disorders E75.23 Krabbe's Disease

Genetic Disorders E75.29 Other sphingolipidosis (Canavan Disease)

Genetic Disorders E75.3 Sphingolipidosis, unspecified

Genetic Disorders E760.1 Hurler Syndrome

Genetic Disorders E760.2 Hurler-Scheie syndrome

Genetic Disorders E760.3 Scheie's syndrome

Genetic Disorders E77.1 Defects in Glycoprotein Degradation (Mannosidosis)

Genetic Disorders E77.8 Other disorders of glycoprotein metabolism

Genetic Disorders E77.9 Disorder of glycoprotein metabolism, unspecified

Genetic Disorders E79.1 Lesch-Nyhan Syndrome

Genetic Disorders E83.00 Disorder of copper metabolism, unspecified Menkes' Syndrome (Kinky Hair Disease)

Genetic Disorders E83.01 Wilson's Disease

Genetic Disorders F84.2 Rett’s Syndrome

Genetic Disorders G31.81 Alper's Disease



ESTABLISHED CONDITION: Genetic Disorders (Continued)


Genetic Disorders G31.82 Leigh’s Disease

Genetic Disorders G70.00 Myasthenia Gravis, without (acute) exacerbation (Familial Infantile)

Genetic Disorders G71.2 Congenital Myopathies

Genetic Disorders G91.1 Obstructive Hydrocephalus

Genetic Disorders M21.511 Acquired clawhand, right hand

Genetic Disorders M21.512 Acquired clawhand, left hand

Genetic Disorders M21.519 Acquired clawhand, unspecified hand

Genetic Disorders M21.521 Acquired clubhand, right hand

Genetic Disorders M21.522 Acquired clubhand, left hand

Genetic Disorders M21.529 Acquired clubhand, unspecified hand

Genetic Disorders M21.531 Acquired clawfoot, right foot

Genetic Disorders M21.532 Acquired clawfoot, left foot

Genetic Disorders M21.539 Acquired clawfoot, unspecified foot

Genetic Disorders M21.541 Acquired Clubfoot, Right Foot

Genetic Disorders M21.542 Acquired Clubfoot, Left Foot

Genetic Disorders M21.549 Acquired Clubfoot, Unspecified Foot (Paralytic Clubbed Foot)

Genetic Disorders M21.511 Acquired clawhand, right hand

Genetic Disorders Q03.1 Atresia of foramina of Magendie and Luschka Dandy Walker Syndrome

Genetic Disorders Q03.9 Congenital hydrocephalus, unspecified

Genetic Disorders Q04.0 Congenital malformations of corpus callosum

Genetic Disorders Q04.3 Other Reduction Deformities of Brain (Polymicrogyria)

Genetic Disorders Q72.10 Congenital Absence of Unspecified limbs

Genetic Disorders Q73.1 Phocomelia, unspecified limb(s)

Genetic Disorders Q73.2 Other Reduction Defects of Unspecified Limb(s)

Genetic Disorders Q75.9 Congenital Anomalies of Skull and Face Bone, unspecified (Goldenhar)

Genetic Disorders Q87.89 Spondyloepiphyseal dysplasia Dyggve-Melchior-Clausen Syndrome (D-M-C Dwarfism)

Genetic Disorders Q78.0 Osteogenesis Imperfecta





Genetic Disorders Q80.8 Other congenital ichthyosis Sjogren-Larsson Syndrome

Genetic Disorders Q85.1 Tuberous Sclerosis

Genetic Disorders Q85.8 Other Phakomatosis, not elsewhere classified (Sturge-Weber Syndrome)

Genetic Disorders E78.72

Congenital malformation syndromes predominantly associated with short stature: (Prader-Willi Syndrome)

Genetic Disorders Q87.89

Congenital malformation syndromes predominantly associated with short stature: (DeLange’s Syndrome)


Congenital malformation syndromes predominantly associated with short stature: (Dubowitz Syndrome)


Congenital malformation syndromes predominantly associated with short stature: (Smith-Lemli-Opitz Syndrome)


Congenital malformation syndromes predominantly involving limbs: (Caudal Regression Syndrome-Sirenomelia)


Congenital malformation syndromes predominantly involving limbs: (Rubinstein-Taybi Syndrome)


Other specified congenital malformation syndromes, not elsewhere classified Zellweger/Cerebrohepatorenal Syndrome

Genetic Disorders Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction)

Genetic Disorders Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)

Genetic Disorders Q90.2 Trisomy 21, translocation

Genetic Disorders Q90.9 Down Syndrome, Unspecified




Genetic Disorders Q91.3 Trisomy 18, Unspecified (Edward's, E3)








Genetic Disorders Q91.7 Trisomy 13, Unspecified (Patau's, D1)

Genetic Disorders Q93.4 Deletion of short arm of chromosome 5(Cri Du Chat or Cat's Cry)

Genetic Disorders Q93.5 Other deletions of part of a chromosome (Angelman's Syndrome)


Other deletions from the autosomes Williams Syndrome

Genetic Disorders Q99.2 Fragile X Syndrome For Boys

Genetic Disorders R47.01 Aphasia



ESTABLISHED CONDITION: Neurologic/Musculoskeletal



Neurologic/Musculoskeletal A80.39 Paralysis, Other Specified

Neurologic/Musculoskeletal G06.2 Extradural and Subdural Abscess, Unspecified (Hemiplegia (Hemiparesis)

Neurologic/Musculoskeletal G11.9 Hereditary Ataxia, Unspecified (Spinocerebellar Disorders)

Neurologic/Musculoskeletal G24.1 Genetic Torsion Dystonia (Dystonia Musculorum Deformans)

Neurologic/Musculoskeletal G25.3 Myoclonus

Neurologic/Musculoskeletal G31.89 Other Specified Degenerative Diseases of Nervous System

Neurologic/Musculoskeletal G60.9 Hereditary and Idiopathic Neuropathy, Unspecified

Neurologic/Musculoskeletal G71.0 Muscular Dystrophy

Neurologic/Musculoskeletal G71.11 Myotonic Muscular Dystrophy

Neurologic/Musculoskeletal G71.12 Myotonia Congenita (Thomsen's Disease)

Neurologic/Musculoskeletal G71.2 Congenital Myopathies

Neurologic/Musculoskeletal G80.0 Spastic quadriplegic cerebral palsy

Neurologic/Musculoskeletal G80.1 Spastic Diplegic Cerebral Palsy (Congenital Diplegia, Paraplegia)

Neurologic/Musculoskeletal G80.2

Spastic hemiplegic cerebral palsy (Congenital Hemiplegia) (Infantile Postnatal NOS) (Spastic Infantile Paralysis)

Neurologic/Musculoskeletal G80.3 Athetoid cerebral palsy

Neurologic/Musculoskeletal G80.4 Ataxic cerebral palsy

Neurologic/Musculoskeletal G80.8 Other cerebral palsy

Neurologic/Musculoskeltal G80.9 Cerebral palsy, unspecified

Neurologic/Musculoskeletal G82.20 Paraplegia, unspecified Paralysis of Both Lower Limbs (Paraplegia)


Quadriplegia, unspecified Paralysis of All Four Limbs (Quadriplegia, Quadriparesis,)

Neurologic/Musculoskeletal G83.0 Diplegia of upper limbs Paralysis of Both Upper Limbs (Diplegia)



ESTABLISHED CONDITION: Neurologic/Musculoskeletal (Continued)



Monoplegia of lower limb affecting unspecified side Paralysis of One Lower Limb (Monoplegia)


Monoplegia of upper limb affecting unspecified side Paralysis of One Upper Limb (Monoplegia)

Neurologic/Musculoskeletal G83.9 Paralytic syndrome, unspecified

Neurologic/Musculoskeletal G93.0 Cerebral Cysts

Neurologic/Musculoskeletal G93.5 Compression of Brain

Neurologic/Musculoskeletal G93.40 Encephalopathy, unspecified

Neurologic/Musculoskeletal G93.49 Other encephalopathy

Neurologic/Musculoskeletal P11.5 Birth injury to spine and spinal cord

Neurologic/Musculoskeletal P90 Convulsions in newborn

Neurologic/Musculoskeletal P91.60 Hypoxic ischemic encephalopathy [HIE], unspecified

Neurologic/Musculoskeletal P94.2 Congenital hypotonia

Neurologic/Musculoskeletal Q00.0 Anencephaly

Neurologic/Musculoskeletal Q01.9 Encephalocele, Unspecified

Neurologic/Musculoskeletal Q02 Microcephaly

Neurologic/Musculoskeletal Q04.2 Holoprosencephaly

Neurologic/Musculoskeletal Q04.3 Other reduction deformities of brain Lissencephaly

Neurologic/Musculoskeletal Q04.6 Congenital cerebral cysts Cortical Dysplasia

Neurologic/Musculoskeletal Q05.8 Sacral spina bifida without hydrocephalus (Meningomyelocele, Meningocele)

Neurologic/Musculoskeletal Q05.9 Spina Bifida, Unspecified

Neurologic/Musculoskeletal Q07.00 Sacral Spina Bifida Without Hydrocephalus

Neurologic/Musculoskeletal Q07.01 Arnold-Chiari Syndrome with Spina Bifida

Neurologic/Musculoskeletal Q07.03 Arnold-Chiari syndrome with spina bifida and hydrocephalus

Neurologic/Musculoskeletal Q76.49 Other congenital malformations of spine, not associated with scoliosis (Sacral Agenesis)

Neurologic/Musculoskeletal Please refer to your medical professional Traumatic Brain Injury



ESTABLISHED CONDITION: Perinatal Factors



Perinatal Factors P07.22 Extreme immaturity of newborn, gestational age 23 completed weeks





Perinatal Factors P07.31 Preterm newborn, gestational age 28 completed weeks

Perinatal Factors P35.0 Congenital rubella syndrome

Perinatal Factors P39.9 Infection specific to the perinatal period, unspecified

Perinatal Factors P84 Other Problems with Newborns (birth asphyxia NOS, Severe)

Perinatal Factors P91.0 Neonatal cerebral ischemia

Perinatal Factors P91.1 Acquired periventricular cysts of newborn

Perinatal Factors P91.2 Neonatal cerebral leukomalacia

Perinatal Factors P91.4 Neonatal Cerebral Depression

Perinatal Factors P91.5 Neonatal Coma

Perinatal Factors P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction



ESTABLISHED CONDITION: Physical Impairments



Physical Impairments C69.01 Malignant neoplasm of right conjunctiva (Retinoblastoma)

Physical Impairments C69.02 Malignant neoplasm of left conjunctiva (Retinoblastoma)

Physical Impairments H33.001 Unspecified retinal detachment with retinal break, right eye

Physical Impairments Q11.1 Other Anophthalmos

Physical Impairments Q11.2 Microphthalmia

Physical Impairments Q13.1 Absence of Iris (Aniridia)

Physical Impairments Q13.89 Other congenital malformations of anterior segment of eye

Physical Impairments Q16.1 Congenital absence, atresia and stricture of auditory canal (external)

Physical Impairments Q17.2 Microtia

Physical Impairments Q17.8 Other specified congenital anomalies of ear

Physical Impairments Q67.8 Other congenital deformities of chest

Physical Impairments Q74.9 Unspecified Congenital Malformation of Limb(s)



ESTABLISHED CONDITION: Sensory Abnormalities



Sensory Abnormalities H26.009 Unspecified Infantile and Juvenile Cataract, Unspecified Eye

Sensory Abnormalities H27.03 Aphakia Bilateral

Sensory Abnormalities H27.03 Aphakia. Bilateral

Sensory Abnormalities H33.009 Unspecified Retinal Detachment with Retinal Break, Unspecified eye

Sensory Abnormalities H35.029 Exudative Retinopathy, Unspecified Eye

Sensory Abnormalities H35.119 Retinopathy of Prematurity, Stage 0, Unspecified Eye






Sensory Abnormalities H35.179 Retrolental Fibroplasia, Unspecified Eye (ROP)

Sensory Abnormalities H35.52 Pignentary Retinal Distrophy (RP)

Sensory Abnormalities H35.54

Dystrophies Primarily Involving the Retinal Pigment Epithelium/Leber’s Congenital Amaurosis

Sensory Abnormalities H47.039 Optic Nerve Hypoplasia, Unspecified Eye

Sensory Abnormalities H47.20 Unspecified Optic Atrophy

Sensory Abnormalities H47.619 Cortical Blindness, Unspecified Side of the Brain (Disorders of visual cortex)

Sensory Abnormalities H53.40 Unspecified Visual Field Defects

Sensory Abnormalities H53.469 Homonomymous Bilateral Field Defects, Unspecified Side



ESTABLISHED CONDITION: Sensory Abnormalities (continued)


Sensory Abnormalities H53.47 Heteronymous Bilateral Field Defects

Sensory Abnormalities H53.51 Achromatopsia

Sensory Abnormalities H54.7 Cortical Visual Impairment (CVI) (Unspecified Visual Loss)

Sensory Abnormalities H54.8 Blindness

Sensory Abnormalities H55.00 Unspecified nystagmus

Sensory Abnormalities H55.01 Congenital nystagmus

Sensory Abnormalities H55.09 Other Forms of Nystagmus

Sensory Abnormalities H90.3 Sensorineural Hearing Loss, Bilateral

Sensory Abnormalities H90.41 Sensorineural Hearing Loss, Unilateral, Right Ear, with Unrestricted Hearing on the Contralateral Side

Sensory Abnormalities H90.42 Sensorineural Hearing Loss, Unilateral, Left Ear, with Unrestricted Hearing on the Contralateral Side

Sensory Abnormalities H90.5 Unspecified Sensorineural Hearing Loss

Sensory Abnormalities H90.8 Mixed Conductive and Sensorineural Hearing Loss, Unspecified

Sensory Abnormalities H90.6 Mixed conductive and sensorineural hearing loss, bilateral


Mixed conductive and sensorineural hearing loss, unilateral, right ear, with

unrestricted hearing on the contralateral side


Mixed conductive and sensorineural hearing loss, unilateral, left ear, with unrestricted

hearing on the contralateral side

Sensory Abnormalities H91.90 Unspecified Hearing Loss, Unspecified Ear

Sensory Abnormalities H91.91 Unspecified hearing loss, right ear

Sensory Abnormalities H91.92 Unspecified hearing loss, left ear



ESTABLISHED CONDITION: Sensory Abnormalities (continued)

Sensory Abnormalities H91.93 Unspecified hearing loss, bilateral

Sensory Abnormalities Q15.0 Congenital Glaucoma

Sensory Abnormalities Q16.9 Congenital Malformations of Ear Causing Impairment of hearing, Unspecified

Sensory Abnormalities Q89.8 Other Specified Congenital Malformations



MEDICAL/BIOLOGICAL RISK CONDITION: Genetic Disorders

A diagnosed physical, mental, or neurobiological condition. The biological or medical risk condition shall be diagnosed by a health care provider and documentation shall be kept on file. Biological and medical risk conditions include the following: (NMAC 7.30.8.10.9 Requirements for Family Infant Toddler Early Intervention Services.) *Questions Regarding conditions not on this list shall be directed to your FIT Manager who will work with a Department of Health Physician to determine whether a proposed condition will be recognized.


Genetic Disorders D82.1 Di George's Syndrome

Genetic Disorders E00.9 Congenital iodine-deficiency syndrome, unspecified

Genetic Disorders E70.0 Classical phenylketonuria

Genetic Disorders E70.30 Albinism, unspecified

Genetic Disorders E71.0 Maple Syrup Urine Disease

Genetic Disorders E71.110 Isovaleric Acidemia

Genetic Disorders E71.121 Methylmalonic Aciduria

Genetic Disorders E71.522 Adrenomyeloneuropathy

Genetic Disorders E72.09 Other disorders of amino-acid transport (Fanconi (-de Toni) (-Debre) Syndrome)

Genetic Disorders E72.11 Homocystinuria

Genetic Disorders E72.22 Argininosuccinic Aciduria

Genetic Disorders E72.51 Non-ketotic hyperglycinemia

Genetic Disorders E74.02 Pompe's Disease

Genetic Disorders E74.21 Galactosemia

Genetic Disorders E75.02 Tay-Sachs disease

Genetic Disorders E77.0 Defects in Post Translational Modification of Lysosomal Enzymes



MEDICAL/BIOLOGICAL RISK CONDITION: Genetic Disorders (continued)


Genetic Disorders E75.19 Other gangliosidosis

Genetic Disorders E75.22 Gaucher’s Disease

Genetic Disorders E75.240 Niemann-Pick disease type A

Genetic Disorders E75.25 Metachromatic Leukodystrophy

Genetic Disorders E75.4 Neuronal Ceroid Lipofuscinoses

Genetic Disorders E75.01 Sandhoff disease

Genetic Disorders F19.939 Other psychoactive substance use, unspecified with withdrawal, unspecified

Genetic Disorders G11.3 Cerebellar ataxia with defective DNA repair

Genetic Disorders G12.0 Infantile Spinal Muscular Atrophy Werdnig-Hoffman Disease,

Genetic Disorders G60.9 Hypertrophic Interstitial Neuritis

Genetic Disorders G90.1 Familial Dysautonomia (Riley-Day Syndrome, HSAN III)

Genetic Disorders I67.9 Cerebrovascular Disease, Unspecified

Genetic Disorders Q79.6 Cutis laxa senilis

Genetic Disorders L94.0 Linear scleroderma

Genetic Disorders P02.8 Newborn (suspected to be) affected by other abnormalities of membranes

Genetic Disorders P35.1 Congenital cytomegalovirus infection

Genetic Disorders P35.1 Congenital cytomegalovirus infection



MEDICAL/BIOLOGICAL RISK CONDITION: Genetic Disorders (continued)


Genetic Disorders G93.89 Other Conditions of the Brain

Genetic Disorders Q06.2 Diastematomyelia

Genetic Disorders Q26.2 Total anomalous pulmonary venous connection


Other specified congenital musculoskeletal deformities (Beals-Hecht Syndrome)

Genetic Disorders Q74.8 Other specified congenital malformations of limb(s) Larsen's Syndrome

Genetic Disorders Q77.0 Achondrogenesis

Genetic Disorders Q77.4 Achondroplasia

Genetic Disorders Q77.5 Diastrophic Dysplasia


Other osteochondrodysplasia with defects of growth of tubular bones and spine Kniest's Syndrome (Metatrophic Dwarfism II)

Genetic Disorders Q78.8 Other Specified Osteochondrodysplasia (Acrodysplasia I)

Genetic Disorders Q78.9 Osteochondrodysplasia, unspecified

Genetic Disorders Q79.6 Ehlers-Danlos Syndrome

Genetic Disorders Q80.9 Congenita Ichthyosis, Unspecified (Harlequin Fetus)

Genetic Disorders Q82.1 Xeroderma Pigmentosum

Genetic Disorders Q85.01 Other Neurofibromatosis


Congenital malformation syndromes predominantly affecting facial appearance Apert's Syndrome (Acrocephalosyndactyly I, ACS I)


Congenital malformation syndromes predominantly affecting facial appearance Saethre-Chotzen Syndrome (Chotzen's, Acrocephalosyndactyly III)



MEDICAL/BIOLOGICAL RISK CONDITION: Genetic Disorders (Continued)



Congenital malformation syndromes predominantly affecting facial appearance Robin’s Syndrome


Congenital malformation syndromes predominantly affecting facial appearance Oral-Facial-Digital Syndrome


Congenital malformation syndromes predominantly associated with short stature Noonan's Syndrome


Congenital malformation syndromes predominantly associated with short stature Russell (-Silver) Syndrome


Congenital malformation syndromes predominantly involving limbs Holt-Oram (Cardiac-Limb) Syndrome (Atriodigital Dysplasia) (Klippel-Trenaunay-Weber Syndrome) Otopalatodigital Syndrome


Congenital malformation syndromes predominantly involving limbs Klippel-Trenaunay-Weber Syndrome


Congenital malformation syndromes predominantly involving limbs Otopalatodigital Syndrome


Congenital malformation syndromes predominantly involving limbs Otopalatodigital Syndrome

Genetic Disorders Q87.2 Congenital malformation syndromes predominantly involving limbs VATER Syndrome

Genetic Disorders Q87.2 Congenital malformation syndromes predominantly involving limbs VATER Syndrome


Congenital malformation syndromes involving early overgrowth Cerebral Gigantism (Soto's Syndrome)

Genetic Disorders Q87.40 Marfan's Syndrome, Unspecified


Other specified congenital malformation syndromes, not elsewhere classified Langer-Giedion Syndrome (Acrodysplasia V, Klingmuller's)

Genetic Disorders Q89.8 Other Specified Congenital Malformations CHARGE Syndrome (CHARGE Association)



MEDICAL/BIOLOGICAL RISK CONDITION: Genetic Disorders (Continued)


Genetic Disorders Q92.8 Other specified trisomies and partial trisomies of autosomes

Genetic Disorders Q93.7 Deletions with other complex rearrangements

Genetic Disorders Q93.81 Velo-cardio-facial Syndrome

Genetic Disorders Q96.9 Turner's syndrome, unspecified

Genetic Disorders Q97.8 Other specified sex chromosome abnormalities, female phenotype

Genetic Disorders Q98.4 Klinefelter syndrome, unspecified

Genetic Disorders Q98.8 Other specified sex chromosome abnormalities, male phenotype

Genetic Disorders Q99.9 Chromosomal Abnormality, Unspecified, (Coffin-Lowry Syndrome)

Genetic Disorders R62.7 Failure to thrive (child)



MEDICAL/BIOLOGICAL RISK CONDITION: Mental/Psychosocial Disorders

A diagnosed physical, mental, or neurobiological condition. The biological or medical risk condition shall be diagnosed by

a health care provider and documentation shall be kept on file. Biological and medical risk conditions include the

following: (NMAC 7.30.8.10.9 Requirements for Family Infant Toddler Early Intervention Services.)

*Questions Regarding conditions not on this list shall be directed to your FIT Manager who will work with a Department of Health Physician to determine whether a proposed condition will be recognized.


Mental/Psychosocial Disorders F32.0

Major Depressive Affective Disorder Single Episode Unspecified (DC 0-3 R: 231 Type I Major Depression)

Mental/Psychosocial Disorders F39

Episodic Mood Disorder Unspecified (DC 0-3 R: 231 Type II Depressive Disorder)

Mental/Psychosocial Disorders F40.10 Social Phobia, Unspecified (DC 0-3 R: 220's Anxiety Disorder Disorder)

Mental/Psychosocial Disorders F40.8 Other Phobic Anxiety Disorders (DC 0-3 R: 220's Anxiety Disorder Disorder)

Mental/Psychosocial Disorders F41.1 Generalized Anxiety Disorder (DC 0-3 R: 220's Anxiety Disorder Disorder)

Mental/Psychosocial Disorders F41.9 Anxiety Disorder, unspecified (DC 0-3 R: 225 Anxiety Disorder NOS)


Post-traumatic stress disorder, unspecified (DC 0-3 R: 100 Post Traumatic Stress Disorder)

Mental/Psychosocial Disorders F43.20 Adjustment disorder, unspecified (DC 0-3 R: 300 Adjustment Disorder)


Adjustment disorder with depressed mood (DC 0-3 R: 210 Prolonged Bereavement/Grief Reaction)

Mental/Psychosocial Disorders F43.22 Adjustment disorder with anxiety (DC 0-3 R: 300 Adjustment Disorder)


Adjustment disorder with mixed anxiety and depressed mood (DC 0-3 R: 300 Adjustment Disorder)


Adjustment disorder with disturbance of conduct (DC 0-3 R: 400's Regulation Disorder of Sensory Processing)



MEDICAL/BIOLOGICAL RISK CONDITION: Mental/Psychosocial Disorders (Continued)



Adjustment disorder with mixed disturbance of emotions and conduct (DC 0-3 R: 150 Deprivation /Maltreatment Disorder or DC 0-3 R: 900 Relationship Disorder If PIR-GAS of 40 or below)

Mental/Psychosocial Disorders F50.00 Anorexia Nervosa, Unspecified (DC 0-3 R: 600's Feeding Behavior Disorder)

Mental/Psychosocial Disorders F50.2 Bulimia Nervosa (DC 0-3 R: 600's Feeding Behavior Disorder)

Mental/Psychosocial Disorders F50.9 Eating disorder, unspecified (DC 0-3 R: 600's Feeding Behavior Disorder)

Mental/Psychosocial Disorders F51.02 Adjustiment Insominia (DC 0-3 R: 500's Sleep Behavior Disorder)


Other insomnia not due to a substance or known physiological condition (DC

0-3 R: 500's Sleep Behavior Disorder)


Other Specified Pervasive Developmental Disorder (DC 0-3 R: 710 Multisystem Development Disorder)


Separation anxiety disorder of childhood (DC 0-3 R: 220's Anxiety Disorder Disorder)


Childhood emotional disorder, unspecified (DC 0-3 R: 240 Mixed Disorder of Emotional Expressiveness)


Other childhood disorders of social functioning (DC 0-3 R: 300 Adjustment Disorder)

Mental/Psychosocial Disorders F98.21 Rumination Disorder of Infancy (DC 0-3 R: 600's Feeding Behavior Disorder)


Other feeding disorders of infancy and early childhood (DC 0-3 R: 600's Feeding Behavior Disorder)

Mental/Psychosocial Disorders F98.3 PICA of Infancy and Childhood (DC 0-3 R: 600's Feeding Behavior Disorder)



MEDICAL/BIOLOGICAL RISK CONDITION: Neurologic/Musculoskeletal



Neurologic/Musculoskeletal A87.9 Viral meningitis, unspecified

Neurologic/Musculoskeletal C72.9 Malignant neoplasm of central nervous system, unspecified

Neurologic/Musculoskeletal G03.9 Meningitis, Unspecified

Neurologic/Musculoskeletal

G40.001

Localization-related (focal) (partial) idiopathic epilepsy and epileptic

syndromes with seizures of localized onset, not intractable, with status

epilepticus


G40.009


syndromes with seizures of localized onset, not intractable, without status

epilepticus


G40.011 Localization-related (focal) (partial) idiopathic epilepsy and epileptic

syndromes with seizures of localized onset, intractable, with status epilepticus


G40.019


syndromes with seizures of localized onset, intractable, without status

epilepticus


G40.111 Localization-related (focal) (partial) symptomatic epilepsy and epileptic

syndromes with simple partial seizures, not intractable, with status epilepticus

https://www.cms.gov/medicare-coverage-database/staticpages/icd-10-code-lookup.aspx?KeyWord=epilepsy&bc=AAAAAAAAAAACAA%3d%3d&







MEDICAL/BIOLOGICAL RISK CONDITION: Neurologic/Musculoskeletal (continued)



G40.109

Localization-related (focal) (partial) symptomatic epilepsy and epileptic

syndromes with simple partial seizures, not intractable, without status

epilepticus



syndromes with simple partial seizures, intractable, with status epilepticus


G40.011


syndromes with complex partial seizures, not intractable, with status

epilepticus


G40.009


syndromes with complex partial seizures, not intractable, without status

epilepticus



syndromes with complex partial seizures, intractable, with status epilepticus



syndromes with complex partial seizures, intractable, without status epilepticus


G40.301 Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with

status epilepticus


G40.309 Generalized idiopathic epilepsy and epileptic syndromes, not intractable,

without status epilepticus














G40.A11 Generalized idiopathic epilepsy and epileptic syndromes, intractable, with

status epilepticus


G40.A19 Generalized idiopathic epilepsy and epileptic syndromes, intractable, without

status epilepticus


G40.821 Other generalized epilepsy and epileptic syndromes, not intractable, with status

epilepticus


G40.822 Other generalized epilepsy and epileptic syndromes, not intractable, without

status epilepticus


G40.823 Other generalized epilepsy and epileptic syndromes, intractable, with status

epilepticus


G40.824 Other generalized epilepsy and epileptic syndromes, intractable, without status

epilepticus

Neurologic/Musculoskeletal G40.801 Other epilepsy, not intractable, with status epilepticus

Neurologic/Musculoskeletal G40.802 Other epilepsy, not intractable, without status epilepticus

Neurologic/Musculoskeletal G40.803 Other epilepsy, intractable, with status epilepticus

Neurologic/Musculoskeletal G40.804 Other epilepsy, intractable, without status epilepticus

Neurologic/Musculoskeletal G40.812 Lennox-Gastaut Syndrome (Gastaut's Syndrome)

Neurologic/Musculoskeletal G40.901 Epilepsy, unspecified, not intractable, with status epilepticus
















Neurologic/Musculoskeletal G40.909 Epilepsy, unspecified, not intractable, without status epilepticus

Neurologic/Musculoskeletal G40.911 Epilepsy, unspecified, intractable, with status epilepticus

Neurologic/Musculoskeletal G40.919 Epilepsy, unspecified, intractable, without status epilepticus

Neurologic/Musculoskeletal G40.B01 Juvenile myoclonic epilepsy, not intractable, with status epilepticus

Neurologic/Musculoskeletal G40.B09 Juvenile myoclonic epilepsy, not intractable, without status epilepticus

Neurologic/Musculoskeletal G40.B11 Juvenile myoclonic epilepsy, intractable, with status epilepticus

Neurologic/Musculoskeletal G40.B19 Juvenile myoclonic epilepsy, intractable, without status epilepticus

Neurologic/Musculoskeletal G72.9 Myopathy Unspecified

Neurologic/Musculoskeletal G83.89 Other Specified Paralytic Syndromes

Neurologic/Musculoskeletal G95.0 Syringomyelia and syringobulbia

Neurologic/Musculoskeletal G95.89 Other specified diseases of spinal cord

Neurologic/Musculoskeletal H55.89 Other irregular eye movements (Kinsbourne Syndrome)

Neurologic/Musculoskeletal I61.9 Nontraumatic intracerebral hemorrhage, unspecified

Neurologic/Musculoskeletal P14.0 Erb’s Paralysis due to Birth Injury

Neurologic/Musculoskeletal Q03.8 Other congenital hydrocephalus

Neurologic/Musculoskeletal Q04.6 Congenital cerebral cysts

Neurologic/Musculoskeletal Q04.8 Other Specified Congenital malformations of brain

Neurologic/Musculoskeletal R56.9 Unspecified convulsions












Neurologic/Musculoskeletal S14.3XXA Injury of Brachial Plexus, Initial Encounter

Neurologic/Musculoskeletal S14.3XXD Injury of Brachial Plexus, Subsequent Encounter

Neurologic/Musculoskeletal S14.3XXS Injury of Brachial Plexus, Sequela Encounter


T56.0X1A Toxic Effects of Lead and Its Compounds, accidental (Sequela), Initial

Encounter


T56.0X1A Toxic Effects of Lead and Its Compounds, accidental (unintentional), Initial

Encounter

Neurologic/Musculoskeletal T74.4XXA Shaken infant syndrome, initial encounter

Neurologic/Musculoskeletal T74.4XXD Shaken infant syndrome, subsequent encounter

Neurologic/Musculoskeletal T74.4XXS Shaken infant syndrome, sequela



MEDICAL/BIOLOGICAL RISK CONDITION: Perinatal Factors



Perinatal Factors A33 Tetanus neonatorum

Perinatal Factors E80.7 Disorder of bilirubin metabolism, unspecified

Perinatal Factors O30.109

Triplet pregnancy, unspecified number of placenta and unspecified number of amniotic sacs, unspecified trimester

Perinatal Factors O30.129 Triplet pregnancy with two or more monoamniotic fetuses, unspecified trimester

Perinatal Factors O30.199

Triplet pregnancy, unable to determine number of placenta and number of amniotic sacs, unspecified trimester

Perinatal Factors P00.9 Newborn (suspected to be) affected by unspecified maternal condition

Perinatal Factors P04.3 Newborn (suspected to be) affected by maternal use of alcohol

Perinatal Factors P04.41 Newborn (suspected to be) affected by maternal use of cocaine

Perinatal Factors P04.49 Newborn (suspected to be) affected by maternal use of other drugs of addiction

Perinatal Factors P04.9 Newborn (suspected to be) affected by maternal noxious substance, unspecified

Perinatal Factors P05.00 Newborn light for gestational age, unspecified weight

Perinatal Factors P07.01 Extremely low birth weight newborn, less than 500 grams

Perinatal Factors P07.02 Extremely low birth weight newborn, 500-749 grams

Perinatal Factors P07.03 Extremely low birth weight newborn, 750-999 grams

Perinatal Factors P07.10 Other low birth weight newborn, unspecified weight

Perinatal Factors P07.14 Other low birth weight newborn, 1000-1249 grams



MEDICAL/BIOLOGICAL RISK CONDITION: Perinatal Factors (continued)










Perinatal Factors P09 Abnormal findings on neonatal screening

Perinatal Factors P29.81 Cardiac arrest of newborn

Perinatal Factors P52.0 Intraventricular (nontraumatic) hemorrhage, grade 1, of newborn




Perinatal Factors P52.3 Unspecified intraventricular (nontraumatic) hemorrhage of newborn

Perinatal Factors P52.5 Subarachnoid (nontraumatic) hemorrhage of newborn

Perinatal Factors P61.9 Perinatal hematological disorder, unspecified

Perinatal Factors P70.4 Other neonatal hypoglycemia

Perinatal Factors P84 Other problems with newborn Intrauterine hypoxia

Perinatal Factors P92.9 Feeding problem of newborn, unspecified

Perinatal Factors P93.8 Other reactions and intoxications due to drugs administered to newborn

Perinatal Factors P04.8 Newborn (Suspected to be) affected by other maternal noxious substances



MEDICAL/BIOLOGICAL RISK CONDITION: Physical Impairments



Physical Impairments M06.9 Rheumatoid arthritis, unspecified

Physical Impairments M41.20 Other idiopathic scoliosis, site unspecified

Physical Impairments Q68.0 Congenital Torticollis

Physical Impairments Q35.9 Cleft palate, unspecified

Physical Impairments Q36.0 Cleft Lip, Bilateral

Physical Impairments Q36.9 Cleft Lip, unilateral

Physical Impairments Q37.9 Cleft Palate with Cleft Lip

Physical Impairments Q71.60 Lobster-claw hand, unspecified hand

Physical Impairments Q71.61 Lobster-Claw Right Hand

Physical Impairments Q71.62 Lobster-Claw Left Hand

Physical Impairments Q71.63 Lobster-Claw Hand, Bilateral

Physical Impairments Q73.8 Other Reduction Defects of Unspecified Limbs

Physical Impairments Q74.3 Arthrogryposis multiplex congenita

Physical Impairments Q74.9 Unspecified Congenital Malformation of Limb(s)

Physical Impairments Q75.0 Craniosynostosis

Physical Impairments Q75.4 Mandibulofacial Dysostosis (Franschetti-Klein Syndrome)

Physical Impairments Q79.0 Congenital Diaphragmatic Hernia

Physical Impairments Q79.3 Gastronschisis

Physical Impairments Q79.4 Prune Belly Syndrome

Physical Impairments Q79.8 Other Congenital Malformations of Musculoskeletal System Poland’s Syndrome

Physical Impairments Q87.0

Congenital Malformation Syndrome Predominantly Affecting Facial Appearance Goldenhar’s Syndrome (Oculouriculoverterbral Dysplasia)0



MEDICAL/BIOLOGICAL RISK CONDITION: Sensory Abnormalities



Sensory Abnormalities F98.4 Stereotyped Movement Disorder (Spasmus Nutans)

Sensory Abnormalities H02.401 Unspecified ptosis of right eyelid

Sensory Abnormalities H02.402 Unspecified ptosis of left eyelid

Sensory Abnormalities H02.403 Unspecified ptosis of bilateral eyelids

Sensory Abnormalities H50.00 Esotropia Unspecified

Sensory Abnormalities H50.10 Exotropia Unspecified

Sensory Abnormalities H50.811 Duane’s Syndrome, Right Eye

Sensory Abnormalities H50.812 Duane’s Syndrome, Left Eye

Sensory Abnormalities H50.89 Other Specified Strabismus

Sensory Abnormalities H51.9 Unspecified disorder of binocular movement

Sensory Abnormalities H52.00 Hypermetropia, unspecified eye

Sensory Abnormalities H52.01 Hypermetropia, right eye

Sensory Abnormalities H52.02 Hypermetropia, left eye

Sensory Abnormalities H52.03 Hypermetropia, bilateral

Sensory Abnormalities H52.13 Myopia, Bilateral

Sensory Abnormalities H52.10 Myopia, unspecified eye



MEDICAL/BIOLOGICAL RISK CONDITION: Sensory Abnormalities (Continued)


Sensory Abnormalities H52.11 Myopia, right eye

Sensory Abnormalities H52.12 Myopia, left eye

Sensory Abnormalities H53.001 Unspecified amblyopia, right eye

Sensory Abnormalities H53.002 Unspecified amblyopia, left eye

Sensory Abnormalities H53.003 Unspecified amblyopia, bilateral

Sensory Abnormalities H53.009 Unspecified Amblyopia

Sensory Abnormalities H53.8 Other visual disturbances

Sensory Abnormalities H53.9 Unspecified Visual Disturbance

Sensory Abnormalities H53.9 unspecified visual loss (Delayed Visual Maturation)

Sensory Abnormalities H65.20 Chronic serous otitis media, unspecified ear

Sensory Abnormalities H65.21 Chronic serous otitis media, right ear

Sensory Abnormalities H65.22 Chronic serous otitis media, left ear

Sensory Abnormalities H65.23 Chronic serous otitis media, bilateral

Sensory Abnormalities H90.2 Conductive hearing loss, unspecified

Sensory Abnormalities Q10.0 Congenital ptosis

Sensory Abnormalities Q17.9 Congenital malformation of ear, unspecified



ENVIRONMENTAL RISK FACTORS: Personal History Presenting Hazard to Health

A presence of adverse family factors in the child’s environment that increases the risk for developmental delay in children. Eligibility determination shall be made using the Environmental Risk Assessment (ERA) tool approved by the FIT program. (NMAC 7.30.8.10.9 Requirements for Family Infant Toddler Early Intervention Services.)


Personal History Presenting Hazard to Health Z77.011 Contact with and (suspected) exposure to lead

Personal History Presenting Hazard to Health Z77.9

Other contact with and (suspected) exposures hazardous to health


Personal history of adult physical and sexual abuse (e.g., sexual abuse or rape)

Personal History Presenting Hazard to Health Z91.412 Personal history of adult neglect (e.g., neglect)


Other personal history of psychological trauma, not elsewhere classified

Personal History Presenting Hazard to Health Z77.9 Other specified personal risk factors, not elsewhere classified

ENVIRONMENTAL RISK FACTORS: Family History of Certain Chronic Disabling Diseases



Family History of Certain Chronic Disabling Diseases Z81.8

Family history of other mental and behavioral disorders


Family history of epilepsy and other diseases of the nervous system


Family history of other diseases of the musculoskeletal system and connective tissue



ENVIRONMENTAL RISK FACTORS: Family History of Certain Other Specific Conditions



Family History of Certain Other Specific Conditions Z81.0 Family History of Intellectual Disabilities

ENVIRONMENTAL RISK FACTORS: Family History of Other Conditions



Family History of Other Conditions Z82.1 Family history of blindness and visual loss

Family History of Other Conditions Z82.2 Family history of deafness and hearing loss

Family History of Other Conditions Z82.79

Family history of other congenital malformations, deformations and chromosomal abnormalities

Family History of Other Conditions Z84.89 Family history of other specified conditions

ENVIRONMENTAL RISK FACTORS: Health Supervision of Infant or Child



Health Supervision of Infant or Child Z76.2

Encounter for health supervision and care of other healthy infant and child (e.g., supervision of healthy infant in cases of socioeconomic adverse condition at home)



ENVIRONMENTAL RISK FACTORS: Housing, Household, and Economic Circumstances



Housing, Household, and Economic Circumstances Z59.0 Homelessness (e.g., Social migrants, Transients)

Housing, Household, and Economic Circumstances Z59.1

Inadequate housing (e.g., Lack of heating, Restriction of space)

Housing, Household, and Economic Circumstances Z59.6 Low income (e.g., Economic problem, Poverty)


Other problems related to housing and economic circumstances

Housing, Household, and Economic Circumstances Z59.9 Unspecified housing or economic circumstance


Need for assistance at home and no other household member able to render care

ENVIRONMENTAL RISK FACTORS: Other Family Circumstances



Other Family Circumstances Z62.898

Other specified problems related to upbringing (e.g., Problem concerning

adopted or foster child)


Dependent relative needing care at home (e.g., Care of sick or handicapped person in family or household)

Other Family Circumstances Z63.72 Alcoholism and drug addiction in family

Other Family Circumstances Z62.891 Other specified problems related to primary support group


Encounter for mental health services for perpetrator of parental child abuse Counseling for parent-child problem, unspecified



ENVIRONMENTAL RISK FACTORS: Other Family Circumstances (Continued)



Encounter for mental health services for victim of parental child abuse Counseling for victim of child abuse


Encounter for mental health services for victim of spousal or partner abuse (Counseling for victim of spousal and partner abuse)


Encounter for mental health services for perpetrator of spousal or partner

abuse (Counseling for perpetrator of spousal and partner abuse)


Other specified counseling (Counseling for marital and partner problems, unspecified)

ENVIRONMENTAL RISK FACTORS: Other Psychosocial Circumstances



Other Psychosocial Circumstances Z13.4 Encounter for screening for certain developmental disorders in childhood

Other Psychosocial Circumstances Z60.3

Acculturation difficulty (e.g., Cultural deprivation, Social isolation or persecution)

Other Psychosocial Circumstances Z63.9 Problem related to primary support group, unspecified

Other Psychosocial Circumstances Z65.3 Problems related to other legal circumstances (e.g., Imprisonment)


Other specified problems related to psychosocial circumstances (e.g., Life circumstance problems)


Other specified problems related to psychosocial circumstances (Interpersonal problems, not elsewhere classified)

Other Psychosocial Circumstances Z65.9 Problem related to unspecified psychosocial circumstances

international classification of disease, 10th revision ...diagnostic codes related to family infant...

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