icd-9 code icd-10 code condition/diagnosis 042 b20 human … · 2020-02-16 · 270.2 e70.20...
Post on 06-Jul-2020
0 Views
Preview:
TRANSCRIPT
ICD-9 Code ICD-10 Code Condition/Diagnosis
042 B20 Human immunodeficiency virus [HIV]
disease
046.2 A81.1 Subacute Sclerosing Panencephalitis
190.5 C69.01 Malignant neoplasm of right
conjunctiva (Retinoblastoma)
190.5 C69.02 Malignant neoplasm of left conjunctiva (Retinoblastoma)
192.9 C72.9 Malignant neoplasm of central nervous system, unspecified
225.0 D33.2 Benign Neoplasm of Brain, Unspecified
237.71 Q85.01 Other Neurofibromatosis
243 E00.9 Congenital iodine-deficiency syndrome, unspecified
270 E72.09 Other disorders of amino-acid transport
(Fanconi (-de Toni) (-Debre) Syndrome)
270.1 E70.0 Classical phenylketonuria
270.2 E70.20 Disorder of tyrosine metabolism,
unspecified
270.2 E70.21 Tyrosinemia, (Type I (Tyrosinosisa) and
Type II (Richner-Hanhart Syndrome)
270.2 E70.29 Disorder of tyrosine metabolism,
unspecified
270.2 E70.30 Albinism, unspecified
270.2
E70.8 Other disorders of aromatic amino-acid
metabolism Waardenburg's Syndrome,
Type I
270.2
E70.9 Disorder of aromatic amino-acid
metabolism, unspecified
270.3 E71.0 Maple Syrup Urine Disease
270.3 E71.110 Isovaleric Acidemia
270.3 E71.121 Methylmalonic Aciduria
270.4 E72.11 Homocystinuria
270.6 E72.22 Argininosuccinic Aciduria
270.7 E72.51 Non-ketotic hyperglycinemia
270.8 E72.03 Lowe's Syndrome or (Oculocerebrorenal Syndrome)
271.0 E74.02 Pompe's Disease
271.1 E74.21 Galactosemia
272.7 E75.11 Mucolipidosis IV
272.7 E75.22 Gaucher’s Disease
272.7 E75.240 Niemann-Pick disease type A
272.7 E75.3 Sphingolipidosis, unspecified
272.7 E77.1 Defects in Glycoprotein Degradation
(Mannosidosis)
272.7 E77.9 Disorder of glycoprotein metabolism,
unspecified
272.7 E77.9 Other disorders of glycoprotein
metabolism
275.1 E83.00 Disorder of copper metabolism, unspecified Menkes' Syndrome (Kinky Hair Disease)
275.1 E83.01 Wilson's Disease
277.00 E84.9 Cystic fibrosis, unspecified
277.00 E84.9 Cystic fibrosis, unspecified
277.2 E79.1 Lesch-Nyhan Syndrome
277.4 E80.7 Disorder of bilirubin metabolism, unspecified
277.5 E760.1 Hurler Syndrome
277.5 E760.2 Hurler-Scheie syndrome
277.5 E760.3 Scheie's syndrome
277.82 E71.42 Carnitine deficiency due to inborn
errors of metabolism
277.85 E71.30 Disorder of fatty-acid metabolism,
unspecified
277.85 E71.310
Long Chain Hydroxy Acyl-CoA
Dehydrogenase Deficiency
277.85 E71.311 Medium Chain Acyl-CoA
Dehydrogenase Deficiency (MCAD)
277.86 E71.522 Adrenomyeloneuropathy
279.11 D82.1 Di George's Syndrome
280.9 D50.9 Iron deficiency anemia, unspecified
282.49 D56.8 Other thalassemias
282.60 D57.1 Sickle-cell disease without crisis
282.7 D58.2 Other hemoglobinopathies
292 F19.939
Other psychoactive substance use,
unspecified with withdrawal,
unspecified
296.2 F32.0 Major Depressive Affective Disorder Single Episode Unspecified (DC 0-3 R: 231 Type I Major Depression)
296.9 F39 Episodic Mood Disorder Unspecified (DC 0-3 R: 231 Type II Depressive Disorder)
299.00 F84.0 Autistic Disorder (DC 0-3 R: 710 Multisystem Development Disorder)
299.8 F84.8 Other Specified Pervasive Developmental Disorder (DC 0-3 R: 710 Multisystem Development Disorder)
299.90 F84.9 Pervasive Development Disorder (PDD), Unspecified
300 F41.9 Anxiety Disorder, unspecified (DC 0-3 R: 225 Anxiety Disorder NOS)
300.02 F41.1 Generalized Anxiety Disorder (DC 0-3 R: 220's Anxiety Disorder Disorder)
300.23 F40.10 Social Phobia, Unspecified (DC 0-3 R: 220's Anxiety Disorder Disorder)
300.29 F40.8 Other Phobic Anxiety Disorders (DC 0-3 R: 220's Anxiety Disorder Disorder)
307.1 F50.00 Anorexia Nervosa, Unspecified (DC 0-3 R: 600's Feeding Behavior Disorder)
307.41 F51.02 Adjustiment Insominia (DC 0-3 R: 500's Sleep Behavior Disorder)
307.42 F51.09
Other insomnia not due to a substance
or known physiological condition (DC
0-3 R: 500's Sleep Behavior Disorder)
307.3 F98.4 Spasmus Nutans
307.5 F50.9 Eating disorder, unspecified (DC 0-3 R: 600's Feeding Behavior Disorder)
307.51 F50.2 Bulimia Nervosa (DC 0-3 R: 600's Feeding Behavior Disorder)
307.52 F98.3 PICA of Infancy and Childhood (DC 0-3 R: 600's Feeding Behavior Disorder)
307.53 F98.21 Rumination Disorder of Infancy (DC 0-3 R: 600's Feeding Behavior Disorder)
307.59 F98.29 Other feeding disorders of infancy and early childhood (DC 0-3 R: 600's Feeding Behavior Disorder)
309.1 F43.21
Adjustment disorder with depressed
mood (DC 0-3 R: 210 Prolonged
Bereavement/Grief Reaction)
309.21 F93.0 Separation anxiety disorder of childhood (DC 0-3 R: 220's Anxiety Disorder Disorder)
309.24 F43.22 Adjustment disorder with anxiety (DC 0-3 R: 300 Adjustment Disorder)
309.28 F43.23
Adjustment disorder with mixed anxiety
and depressed mood (DC 0-3 R: 300
Adjustment Disorder)
309.29 F43.29 Other childhood disorders of social functioning (DC 0-3 R: 300 Adjustment Disorder)
309.3 F43.24 Adjustment disorder with disturbance of conduct (DC 0-3 R: 400's Regulation Disorder of Sensory Processing)
309.4 F43.25
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)
309.81 F43.10 Post-traumatic stress disorder, unspecified (DC 0-3 R: 100 Post Traumatic Stress Disorder)
309.9 F43.20 Adjustment disorder, unspecified (DC 0-3 R: 300 Adjustment Disorder)
313.9 F93.9 Childhood emotional disorder, unspecified (DC 0-3 R: 240 Mixed Disorder of Emotional Expressiveness)
315.31 F80.1 Expressive Language Disorder
315.32 F80.2 Mixed Receptive-Expressive Language Disorder
315.35 F80.81 Childhood Onset Fluency Disorder
315.39 F80.89 Other developmental disorders of speech and language
315.4 F82 Specific Developmental Disorder of Motor Functions
315.5 F82 Specific Developmental Disorder of Motor Functions (Mixed Development Disorder)
315.8 F88 Other disorders of psychological development Other Specified Delays in Development
315.9 F81.9 Developmental Disorder of Scholastic Skills (Mixed Development Disorder)
317.0 F70 Mild Intellectual Disabilities
318.0 F71 Moderate Intellectual Disabilities
318.1 F72 Severe Intellectual Disabilities
318.2 F73 Profound Intellectual Disabilities
319.0 F79 Unspecified Intellectual Disabilities
322.9 G03.9 Meningitis Unspecified
324.9 G06.2 Extradural and Subdural Abscess, Unspecified (Hemiplegia (Hemiparesis)
330 E75.25 Metachromatic Leukodystrophy
330.0 E75.23 Krabbe's Disease
330.0 E75.29 Other sphingolipidosis (Canavan
Disease)
330.1 E75.02 Tay-Sachs disease
330.1 E75.19 Other gangliosidosis
330.1 E75.4 Neuronal Ceroid Lipofuscinoses
330.1 E7501 Sandhoff disease
330.8 F84.2 Rett’s Syndrome
330.8 G31.81 Alper's Disease
330.8 G31.82 Leigh’s Disease
331.4 G91.1 Obstructive Hydrocephalus
331.89 G31.89 Other Specified Degenerative Diseases of Nervous System
333.2 G25.3 Myoclonus
333.6 G24.1 Genetic Torsion Dystonia (Dystonia Musculorum Deformans)
334.8 G11.3 Cerebellar ataxia with defective DNA repair
334.9 G11.9 Hereditary Ataxia, Unspecified (Spinocerebellar Disorders)
335 G12.0 Infantile Spinal Muscular Atrophy Werdnig-Hoffman Disease,
336 G95.0 Syringomyelia and syringobulbia
336.6 G95.89 Other specified diseases of spinal cord
343.0 G80.1 Spastic diplegic cerebral palsy
(Congenital Diplegia, Paraplegia)
343.1 G80.2 Cerebral Palsy, Infantile, Hemiplegic
(Congenital Hemiplegia)
343.1 G80.2 Spastic hemiplegic cerebral palsy
Hemiplegia, Congenital (Spastic
Infantile Paralysis)
343.2 G40.301
Generalized idiopathic epilepsy and
epileptic syndromes, not intractable,
with status epilepticus
343.2 G80.0 Spastic quadriplegic cerebral palsy
343.3 G80.8 Other cerebral palsy Cerebral Palsy,
Infantile, Monoplegic
343.4 G80.2 Hemiplegia, Infantile (Postnatal), NOS
343.8 G80.8 Cerebral Palsy, Infantile, Other
Specified
343.9 G80.9 Cerebral Palsy, Infantile, Unspecified
344.0 G82.50 Quadriplegia, unspecified Paralysis of All Four Limbs (Quadriplegia, Quadriparesis,)
344.1 G82.20 Paraplegia, unspecified Paralysis of Both Lower Limbs (Paraplegia)
344.2 G83.0 Diplegia of upper limbs Paralysis of Both Upper Limbs (Diplegia)
344.3 G83.10 Monoplegia of lower limb affecting unspecified side Paralysis of One Lower Limb (Monoplegia)
344.4 G83.20 Monoplegia of upper limb affecting unspecified side Paralysis of One Upper Limb (Monoplegia)
344.89 G83.89 Other Specified Paralytic Syndromes
344.9 G83.9 Paralytic syndrome, unspecified
345.00 G40.309
Generalized idiopathic epilepsy and
epileptic syndromes, not intractable,
without status epilepticus
345.01 G40.319
Generalized idiopathic epilepsy and
epileptic syndromes, intractable,
without status epilepticus
345.5 G40.311
Generalized idiopathic epilepsy and
epileptic syndromes, intractable, with
status epilepticus
345.50 G40.001
Localization-related (focal) (partial)
idiopathic epilepsy and epileptic
syndromes with seizures of localized
onset, not intractable, with status
epilepticus
345.50 G40.009
Localization-related (focal) (partial)
idiopathic epilepsy and epileptic
syndromes with seizures of localized
onset, not intractable, without status
epilepticus
345.50 G40.011
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with complex partial
seizures, not intractable, without status
epilepticus
345.50 G40.119
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with simple partial seizures,
intractable, without status epilepticus
345.50 G40.219
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with complex partial
seizures, intractable, without status
epilepticus
345.50 G40.A19
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with simple partial seizures,
not intractable, without status
epilepticus
345.51 G40.011
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with complex partial
seizures, not intractable, with status
epilepticus
345.51 G40.019
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with complex partial
seizures, intractable, with status
epilepticus
345.51 G40.101
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with simple partial seizures,
not intractable, with status epilepticus
345.51 G40.111
Localization-related (focal) (partial)
idiopathic epilepsy and epileptic
syndromes with seizures of localized
onset, intractable, with status epilepticus
345.51 G40.119
Localization-related (focal) (partial)
idiopathic epilepsy and epileptic
syndromes with seizures of localized
onset, intractable, without status
epilepticus
345.51 G40.A11
Localization-related (focal) (partial)
symptomatic epilepsy and epileptic
syndromes with simple partial seizures,
intractable, with status epilepticus
345.60 G40.821
Other generalized epilepsy and epileptic
syndromes, not intractable, with status
epilepticus
345.60 G40.822
Other generalized epilepsy and epileptic
syndromes, not intractable, without
status epilepticus
345.61 G40.823
Other generalized epilepsy and epileptic
syndromes, intractable, with status
epilepticus
345.61 G40.824
Other generalized epilepsy and epileptic
syndromes, intractable, without status
epilepticus
345.80 G40.801 Other epilepsy, not intractable, with
status epilepticus
345.80 G40.802 Other epilepsy, not intractable, without
status epilepticus
345.80 G40.B01 Juvenile myoclonic epilepsy, not
intractable, with status epilepticus
345.80 G40.B09 Juvenile myoclonic epilepsy, not
intractable, without status epilepticus
345.81 G40.803 Other epilepsy, intractable, with status
epilepticus
345.81 G40.804 Other epilepsy, intractable, without
status epilepticus
345.81 G40.B11 Juvenile myoclonic epilepsy, intractable,
with status epilepticus
345.81 G40.B19 Juvenile myoclonic epilepsy, intractable,
without status epilepticus
345.90 G40.901 Epilepsy, unspecified, not intractable,
with status epilepticus
345.90 G40.909 Epilepsy, unspecified, not intractable,
without status epilepticus
345.91 G40.911 Epilepsy, unspecified, intractable, with
status epilepticus
345.91 G40.919 Epilepsy, unspecified, intractable,
without status epilepticus
348 G93.0 Congenital cerebral cysts
348.0 G93.0 Cerebral Cysts
348.39 G93.49 Other encephalopathy
348.8 G93.89 Other Conditions of the Brain
356.9 G60.9 Hereditary and Idiopathic Neuropathy, Unspecified
356.9 G60.9 Hypertrophic Interstitial Neuritis
358.00 G70.00 Myasthenia Gravis, without (acute) exacerbation (Familial Infantile)
359.0 G71.2 Congenital Myopathies
359.0 G71.2 Congenital Myopathies
359.1 G71.0 Muscular Dystrophy
359.21 G71.11 Myotonic Muscular Dystrophy
359.22 G71.12 Myotonia Congenita (Thomsen's Disease)
359.9 G72.9 Myopathy Unspecified
361.0 H33.001
Unspecified retinal detachment with
retinal break, right eye
361.0 H33.002
Unspecified retinal detachment with
retinal break, left eye
361.0 H33.003
Unspecified retinal detachment with
retinal break, bilateral
361.0 H33.009 Unspecified Retinal Detachment with Retinal Break, Unspecified eye
362.21 H35.179 Retrolental Fibroplasia, Unspecified Eye
362.21 H35171
Retrolental fibroplasia, right eye
362.21 H35172
Retrolental fibroplasia, left eye
362.21 H35173
Retrolental fibroplasia, bilateral
362.12 H35.02
Retinopathy, Exudative
362.22 H35.11
Retonpathy of Prematurity, stage 0
362.23 H35.12
Retonpathy of Prematurity, stage 1
362.24 H35.13
Retonpathy of Prematurity, stage 2
362.25 H35.14
Retonpathy of Prematurity, stage 3
362.26 H35.15
Retonpathy of Prematurity, stage 4
362.27 H35.16
Retonpathy of Prematurity, stage 5
362.74 H35.52 Pigmentary retinal dystrophy
362.76 H35.54 Dystrophies Primarily Involving the Retinal Pigment Epithelium (Leber’s Congenital Amaurosis)
366 H26.001
Unspecified infantile and juvenile
cataract, right eye
366 H26.002
Unspecified infantile and juvenile
cataract, left eye
366 H26.003
Unspecified infantile and juvenile
cataract, bilateral
366 H26.009 Unspecified Infantile and Juvenile Cataract, Unspecified Eye
367 H52.00 Hypermetropia, unspecified eye
367 H52.01 Hypermetropia, right eye
367 H52.02 Hypermetropia, left eye
367 H52.03 Hypermetropia, bilateral
367.1 H52.10 Myopia, unspecified eye
367.1 H52.11 Myopia, right eye
367.1 H52.12 Myopia, left eye
367.1 H52.13 Myopia, Bilateral
368.0 H53.001 Unspecified amblyopia, right eye
368.0 H53.002 Unspecified amblyopia, left eye
368.0 H53.003 Unspecified amblyopia, bilateral
368.0 H53.009 Unspecified Amblyopia
368.4 H53.40 Unspecified Visual Field Defects
368.46 H53.461
Homonymous bilateral field defects,
right side
368.46 H53.462
Homonymous bilateral field defects, left
side
368.46 H53.469 Homonomymous Bilateral Field Defects, Unspecified Side
368.47 H53.47 Heteronymous Bilateral Field Defects
368.54 H53.51 Achromatopsia
368.8 H53.8 Other visual disturbances
368.8 H53.8 Unspecified Visual Disturbance
368.9 H53.9 unspecified visual loss (Delayed Visual Maturation)
369.4 H54.8 Legal blindness, as defined in USA
369.9 H02.315.403 Unspecified ptosis of bilateral eyelids
369.9 H02.401 Unspecified ptosis of right eyelid
369.9 H02.402 Unspecified ptosis of left eyelid
369.9 H54.7 Unspecified Visual Loss
377.1 H47.20 Unspecified Optic Atrophy
377.43 H47.031 Optic nerve hypoplasia, right eye
377.43 H47.032 Optic nerve hypoplasia, left eye
377.43 H47.033 Optic nerve hypoplasia, bilateral
377.43 H47.039 Optic Nerve Hypoplasia, Unspecified Eye
377.75 H47.611 Cortical blindness, right side of brain
377.75 H47.612 Cortical blindness, left side of brain
377.75 H47.619 Cortical Blindness, Unspecified Side of the Brain
378 H50.10 Exotropia Unspecified
378.00 H50.00 Esotropia Unspecified
378.71 H50.811 Duane’s Syndrome, Right Eye
378.71 H50.812 Duane’s Syndrome, Left Eye
378.73 H50.89 Other Specified Strabismus
378.9 H51.9 Unspecified disorder of binocular movement
379.31 H27.03 Aphakia Bilateral
379.5 H55.00 Unspecified nystagmus
379.5 H55.01 Congenital nystagmus
381.10 H65.20 Chronic serous otitis media, unspecified
ear
381.10 H6521 Chronic serous otitis media, right ear
381.10 H6522 Chronic serous otitis media, left ear
381.10 H6523 Chronic serous otitis media, bilateral
389 H90.2 Conductive hearing loss, unspecified
389.14 H90.5 Unspecified Sensorineural Hearing Loss
389.15 H90.41 Sensorineural Hearing Loss, Unilateral, Right Ear, with Unrestricted Hearing on the Contralateral Side
389.15 H90.42 Sensorineural Hearing Loss, Unilateral, Left Ear, with Unrestricted Hearing on the Contralateral Side
389.18 H90.3 Sensorineural Hearing Loss, Bilateral
389.2 H90.6
Mixed conductive and sensorineural
hearing loss, bilateral
389.2
H90.71
Mixed conductive and sensorineural
hearing loss, unilateral, right ear, with
unrestricted hearing on the contralateral
side
389.2
H90.72
Mixed conductive and sensorineural
hearing loss, unilateral, left ear, with
unrestricted hearing on the contralateral
side
389.20 H90.8 Mixed Conductive and Sensorineural Hearing Loss, Unspecified
389.9 H91.90 Unspecified Hearing Loss, Unspecified Ear
389.9 H91.91 Unspecified hearing loss, right ear
389.9 H91.92 Unspecified hearing loss, left ear
389.9 H91.93 Unspecified hearing loss, bilateral
431 I61.9 Nontraumatic intracerebral hemorrhage, unspecified
437.9 I67.9 Cerebrovascular Disease, Unspecified
47.9 A87.9 Viral meningitis, unspecified
536.49 K94.29 Other complications of gastrostomy
651.1 O30.109 Triplet pregnancy, unspecified number of placenta and unspecified number of amniotic sacs, unspecified trimester
714.0 M06.9 Rheumatoid arthritis, unspecified
736.06 M21.511 Acquired clawhand, right hand
736.06 M21.511 Acquired clawhand, right hand
736.06 M21.512 Acquired clawhand, left hand
736.06 M21.519 Acquired clawhand, unspecified hand
736.07 M21.521 Acquired clubhand, right hand
736.07 M21.522 Acquired clubhand, left hand
736.07 M21.529 Acquired clubhand, unspecified hand
736.71 M21.541 Acquired clubfoot, right foot
736.71 M21.542 Acquired clubfoot, left foot
736.71 M21.549 Acquired clubfoot, unspecified foot
736.74 M21.531 Acquired clawfoot, right foot
736.74 M21.532 Acquired clawfoot, left foot
736.74 M21.539 Acquired clawfoot, unspecified foot
737.30 M41.20 Other idiopathic scoliosis, site unspecified
741.00 Q07.03 Arnold-Chiari syndrome with spina bifida and hydrocephalus
741.00 Q07.03 Arnold-Chiari syndrome with spina
bifida and hydrocephalus
741.00 Q0701 Arnold-Chiari syndrome with spina
bifida
741.00 Q0702 Arnold-Chiari syndrome with
hydrocephalus
741.9 Q05.8 Sacral spina bifida without hydrocephalus (Meningomyelocele, Meningocele)
741.90 Q05.9 Spina Bifida, Unspecified
742.0 Q01.9 Encephalocele, Unspecified
742.1 Q02 Microcephaly
742.2 Q04.0 Congenital malformations of corpus callosum
742.2 Q04.2 Holoprosencephaly
742.2 Q04.3 Other Reduction Deformities of Brain (Polymicrogyria)
742.2 Q04.3 Other reduction deformities of brain Lissencephaly
742.3 Q03.1 Atresia of foramina of Magendie and Luschka Dandy Walker Syndrome
742.3 Q03.8 Other congenital hydrocephalus
742.3 Q03.9 Congenital hydrocephalus, unspecified
742.4 Q04.6 Congenital cerebral cysts Cortical Dysplasia
742.4 Q04.6 schizencephaly
742.4 Q04.8 Other Specified Congenital malformations of brain
742.51 Q06.2 Diastematomyelia
742.8 G90.1 Familial Dysautonomia (Riley-Day Syndrome, HSAN III)
742.9 G93.40 Encephalopathy, unspecified
743.0 Q11.1 Other Anophthalmos
743.1 Q11.2 Microphthalmia
743.20 Q15.0 Congenital Glaucoma
743.45 Q13.1 Absence of Iris (Aniridia)
743.49 Q13.89 Other congenital malformations of anterior segment of eye
743.61 Q10.0 Congenital ptosis
744 Q16.9 Congenital Malformations of Ear Causing Impairment of hearing, Unspecified
744.02 Q16.1 Congenital absence, atresia and stricture of auditory canal (external)
744.23 Q17.2 Microtia
744.29 Q17.8 Other specified congenital anomalies of ear
744.3 Q17.9 Congenital malformation of ear, unspecified
746.89 Q23.8 Other Congenital Malformations of Aortic and Mitral Valves
747.41 Q26.2
Total anomalous pulmonary venous
connection
749.00 Q35.9 Cleft palate, unspecified
749.10 Q36.0 Cleft lip, bilateral
749.10 Q36.9 Cleft Lip, unilateral
749.2 Q37.9 Cleft Palate with Cleft Lip
754.1 Q68.0 Congenital Torticollis
754.89 Q67.8 Other congenital deformities of chest
754.89 Q74.3 Arthrogryposis multiplex congenita
755.33 Q73.10 Phocomelia, unspecified limb(s)
755.4 Q73.0 Congenital Absence of Unspecified limbs
755.4 Q73.8 Other Reduction Defects of Unspecified Limbs
755.5 Q74.9 Unspecified Congenital Malformation of Limb(s)
755.50 Q74.9 Unspecified Congenital Malformation of Limb(s)
755.58 Q71.60 Lobster-claw hand, unspecified hand
755.58 Q71.61 Lobster-claw right hand
755.58 Q71.62 Lobster-claw left hand
755.58 Q71.63 Lobster-claw hand, bilateral
755.8 Q74.8 Other specified congenital malformations of limb(s) Larsen's Syndrome
756 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Robin’s Syndrome
756.0 Q75.0 Craniosynostosis
756.0 Q75.4 Mandibulofacial Dysostosis (Franschetti-Klein Syndrome)
756.0 Q75.9 Congenital Anomalies of Skull and Face Bone, unspecified (Goldenhar)
756.0 Q87.0
Congenital malformation syndromes predominantly affecting facial appearance Apert's Syndrome (Acrocephalosyndactyly I, ACS I)
756.0 Q87.0
Congenital malformation syndromes predominantly affecting facial appearance Saethre-Chotzen Syndrome (Chotzen's, Acrocephalosyndactyly III)
756.0 Q87.0
Congenital malformation syndromes predominantly affecting facial appearance Goldenhar's Syndrome (Oculoauriculovertebral Dysplasia)
756.13 Q76.49 Other congenital malformations of spine, not associated with scoliosis (Sacral Agenesis)
756.4 Q77.0 Achondrogenesis
756.4 Q77.4 Achondroplasia
756.4 Q77.5 Diastrophic Dysplasia
756.5 Q78.9 Osteochondrodysplasia, unspecified
756.51 Q78.0 Osteogenesis Imperfecta
756.59 Q78.8 Other Specified Osteochondrodysplasia (Acrodysplasia I)
756.6 Q79.0 Congenital Diaphragmatic Hernia
756.71 Q79.4 Prune Belly Syndrome
756.73 Q79.3 Gastroschisis
756.83 Q79.6 Cutis laxa senilis
756.83 Q79.6 Ehlers-Danlos Syndrome
756.9 Q79.8 Other congenital malformations of musculoskeletal system Poland's Syndrome
756.9 Q79.9 Congenital Malformations of Musculoskeletal System, Unspecified
757.1 Q80.8 Other congenital ichthyosis Sjogren-Larsson Syndrome
757.1 Q80.9 Congenita Ichthyosis, Unspecified (Harlequin Fetus)
757.33 Q82.1 Xeroderma Pigmentosum
758.0 Q90.0 Trisomy 21, nonmosaicism (meiotic
nondisjunction)
758.0 Q90.1 Trisomy 21, mosaicism (mitotic
nondisjunction)
758.0 Q90.2 Trisomy 21, translocation
758.0 Q90.9 Down Syndrome, Unspecified
758.1 Q91.4 Trisomy 13, nonmosaicism (meiotic
nondisjunction)
758.1 Q91.5 Trisomy 13, mosaicism (mitotic
nondisjunction)
758.1 Q91.6 Trisomy 13, translocation
758.1 Q91.7 Trisomy 13, Unspecified (Patau's, D1)
758.2 Q91.0 Trisomy 18, nonmosaicism (meiotic
nondisjunction)
758.2 Q91.1 Trisomy 18, mosaicism (mitotic
nondisjunction)
758.2 Q91.2 Trisomy 18, translocation
758.2 Q91.3 Trisomy 18, Unspecified (Edward's, E3)
758.31 Q93.4 Deletion of short arm of chromosome
5(Cri Du Chat or Cat's Cry)
758.32 Q93.81 Velo-cardio-facial Syndrome
758.39 Q93.7 Deletions with other complex rearrangements
758.5 Q92.8 Other specified trisomies and partial trisomies of autosomes
758.6 Q96.9 Turner's syndrome, unspecified
758.7 Q98.4 Klinefelter syndrome, unspecified
758.8 Q99.8 Other Specified Chromosomal Anomalies
758.81 Q97.8 Other specified sex chromosome abnormalities, female phenotype
758.81 Q98.8 Other specified sex chromosome abnormalities, male phenotype
758.9 Q99.9 Chromosomal Abnormality, Unspecified, (Coffin-Lowry Syndrome)
759.39 Q93.5 Other deletions of part of a chromosome
(Angelman's Syndrome)
759.5 Q85.1 Tuberous Sclerosis
759.6 Q85.8 Other Phakomatosis, not elsewhere
classified (Sturge-Weber Syndrome)
759.81 Q87.1 Congenital malformation syndromes predominantly associated with short stature (Prader-Willi Syndrome)
759.82 Q68.8 Other specified congenital musculoskeletal deformities (Beals-Hecht Syndrome)
759.82 Q87.40 Marfan's Syndrome, Unspecified
759.83 Q99.2 Fragile X Syndrome For Boys
759.83 Q99.2 Fragile X Syndrome For Girls
759.89 E78.72 Congenital malformation syndromes predominantly associated with short stature Smith-Lemli-Opitz Syndrome
759.89 L94.0 Morphea
759.89 Q00.0 Anencephaly
759.89 Q87.0
Congenital malformation syndromes predominantly affecting facial appearance Oral-Facial-Digital Syndrome
759.89 Q87.1
Congenital malformation syndromes predominantly associated with short stature
759.89 Q87.1 Congenital malformation syndromes predominantly associated with short stature Noonan's Syndrome
759.89 Q87.1 Congenital malformation syndromes predominantly associated with short stature Russell (-Silver) Syndrome
759.89 Q87.2 Congenital malformation syndromes predominantly involving limbs Klippel-Trenaunay-Weber Syndrome
759.89 Q87.2 Congenital malformation syndromes predominantly involving limbs -Caudal Regression Syndrome (Sirenomelia)
759.89 Q87.2 Congenital malformation syndromes predominantly involving limbs Otopalatodigital Syndrome
759.89 Q87.2 Congenital malformation syndromes predominantly involving limbs Rubinstein-Taybi Syndrome
759.89 Q87.2 Congenital malformation syndromes predominantly involving limbs VATER Syndrome
759.89 Q87.3 Congenital malformation syndromes involving early overgrowth (Beckwith-Wiedemann Syndrome)
759.89 Q87.3 Congenital malformation syndromes involving early overgrowth Cerebral Gigantism (Soto's Syndrome)
759.89 Q87.89 Congenital malformation syndromes predominantly associated with short stature Dubowitz Syndrome
759.89 Q87.89
Other specified congenital malformation syndromes, not elsewhere classified Zellweger/Cerebrohepatorenal Syndrome
759.89 Q87.89
Other specified congenital malformation
syndromes, not elsewhere classified
(Biedl-Bardet Syndrome)
759.89 Q87.89
Other specified congenital malformation syndromes, not elsewhere classified Langer-Giedion Syndrome (Acrodysplasia V, Klingmuller's)
759.89 Q87.89 Spondyloepiphyseal dysplasia Dyggve-Melchior-Clausen Syndrome (D-M-C Dwarfism)
759.89 Q89.8 Other Specified Congenital Malformations CHARGE Syndrome (CHARGE Association)
759.89 Q93.89 Other deletions from the autosomes
Williams Syndrome
760.70 P04.9 Newborn (suspected to be) affected by maternal noxious substance, unspecified
760.71 P04.3 Newborn (suspected to be) affected by maternal use of alcohol
760.71 Q86.0 Fetal alcohol syndrome (dysmorphic)
760.72 P04.49 Newborn (suspected to be) affected by maternal use of other drugs of addiction
760.75 P04.41 Newborn (suspected to be) affected by maternal use of cocaine
760.79 P04.8 Newborn (suspected to be) affected by other abnormalities of membranes
760.79 Q86.1 Fetal hydantoin syndrome
764.0 P05.00 Newborn light for gestational age, unspecified weight
765.01 P07.01 Extremely low birth weight newborn,
less than 500 grams
765.02 P07.02 Extremely low birth weight newborn, 500-749 grams
765.03 P07.03 Extremely low birth weight newborn, 750-999 grams
765.10 P07.10 Other low birth weight newborn, unspecified weight
765.14 P07.14 Other low birth weight newborn, 1000-1249 grams
765.15 P07.15 Other low birth weight newborn, 1250-1499 grams
765.16 P07.16 Other low birth weight newborn, 1500-1749 grams
765.21 P07.21 Extreme immaturity of newborn, gestational age less than 23 completed weeks
765.21 P07.22 Extreme immaturity of newborn, gestational age 23 completed weeks
765.22 P07.23 Extreme immaturity of newborn, gestational age 24 completed weeks
765.23 P07.24 Extreme immaturity of newborn, gestational age 25 completed weeks
765.23 P07.25 Extreme immaturity of newborn,
gestational age 26 completed weeks
765.24 P07.26 Extreme immaturity of newborn, gestational age 27 completed weeks
765.24 P07.31 Preterm newborn, gestational age 28 completed weeks
765.25 P07.32 Preterm newborn, gestational age 29 completed weeks
765.25 P07.33 Preterm newborn, gestational age 30
completed weeks
765.26 P07.34 Preterm newborn, gestational age 31 completed weeks
765.26 P07.35 Preterm newborn, gestational age 32 completed weeks
765.27 P07.36 Preterm newborn, gestational age 33 completed weeks
765.27 P07.37 Preterm newborn, gestational age 34 completed weeks
767.6 P14.0 Erb’s Paralysis due to Birth Injury
768.6 P84 Other Problems with Newborns (birth asphyxia NOS, Severe)
768.70 P91.60 Hypoxic ischemic encephalopathy [HIE], unspecified
770.88 P84 Other problems with newborn Intrauterine hypoxia
771.0 P35.0 Congenital rubella syndrome
771.1 P35.1 Congenital cytomegalovirus infection
771.2 P39.9 Infection specific to the perinatal period, unspecified
771.3 A33 Tetanus neonatorum
772.10 P52.3 Unspecified intraventricular (nontraumatic) hemorrhage of newborn
772.11 P52.0 Intraventricular (nontraumatic) hemorrhage, grade 1, of newborn
772.12 P52.1 Intraventricular (nontraumatic) hemorrhage, grade 2, of newborn
772.13 P52.21 Intraventricular (nontraumatic) hemorrhage, grade 3, of newborn
772.14 P52.22 Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn
772.2 P52.5 Subarachnoid (nontraumatic) hemorrhage of newborn
772.8 P54.8 Other specified neonatal hemorrhages
775.6 P70.4 Other neonatal hypoglycemia
776.9 P61.9 Perinatal hematological disorder, unspecified
779.0 P90 Convulsions in newborn
779.2 P91.0
Neonatal cerebral ischemia
779.2 P91.1
Acquired periventricular cysts of
newborn
779.2 P91.2 Neonatal cerebral leukomalacia
779.2 P91.4 Neonatal Cerebral Depression
779.2 P91.5 Neonatal Coma
779.31 P92.9 Feeding problem of newborn, unspecified
779.4 P93.8 Other reactions and intoxications due to drugs administered to newborn
779.5 P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction
779.85 P29.81 Cardiac arrest of newborn
780.39 R56.9 Unspecified convulsions
781.3 P94.2 Congenital hypotonia
783.81 R62.7 Failure to thrive (child)
784.3 R47.01 Aphasia
796.6 P09 Abnormal findings on neonatal screening
806.0 P11.5 Birth injury to spine and spinal cord
907.3 T56.0X1A Toxic Effects of Lead and Its Compounds, accidental (unintentional), Initial Encounter
909.9 T74.4XXS Shaken infant syndrome, sequela
953.4 S14.3XXA Injury of Brachial Plexus, Initial Encounter
984.9 T56.0X15 Toxic Effects of Lead and Its Compounds, accidental (Sequela), Initial Encounter
995.55 T74.4XXA Shaken infant syndrome, initial encounter
V11.3 Z65.8
Other specified problems related to psychosocial circumstances (Interpersonal problems, not elsewhere classified)
V15.41 Z91.410 Personal history of adult physical and sexual abuse (e.g., sexual abuse or rape)
V15.42 Z91.412 Personal history of adult neglect (e.g., neglect)
V15.49 Z91.49 Other personal history of psychological trauma, not elsewhere classified
V15.86 Z77.011 Contact with and (suspected) exposure to lead
V15.89 Z77.9 Other contact with and (suspected) exposures hazardous to health
V15.9 Z91.89 Other specified personal risk factors, not elsewhere classified
V17.0 Z81.8 Family history of other mental and behavioral disorders
V17.2 Z82.0 Family history of epilepsy and other diseases of the nervous system
V17.89 Z82.69 Family history of other diseases of the musculoskeletal system and connective tissue
V18.4 Z81.0
Family History of Intellectual Disabilities
V19.0 Z82.1 Family history of blindness and visual loss
V19.2 Z82.2 Family history of deafness and hearing loss
V19.5 Z82.79 Family history of other congenital malformations, deformations and chromosomal abnormalities
V19.8 Z84.89 Family history of other specified conditions
V20.1
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)
V29.9 P00.9 Newborn (suspected to be) affected by unspecified maternal condition
V58.89 S14.3XXD
Injury of Brachial Plexus, Subsequent Encounter
V58.89 T74.4XXD Shaken infant syndrome, subsequent encounter
V60.0 Z59.0 Homelessness (e.g., Social migrants, Transients)
V60.1 Z59.1 Inadequate housing (e.g., Lack of heating, Restriction of space)
V60.2 Z59.6 Low income (e.g., Economic problem, Poverty)
V60.4 Z74.2 Need for assistance at home and no other household member able to render care
V60.89 Z59.8 Other problems related to housing and economic circumstances
V60.9 Z59.9 Unspecified housing or economic circumstance
V61.11 Z69.11
Encounter for mental health services for victim of spousal or partner abuse (Counseling for victim of spousal and partner abuse)
V61.12 Z69.12 Encounter for mental health services for
perpetrator of spousal or partner abuse
(Counseling for perpetrator of spousal
and partner abuse)
V61.21 Z69.010
Encounter for mental health services for perpetrator of parental child abuse Counseling for parent-child problem, unspecified
V61.21 Z69.020 Encounter for mental health services for victim of parental child abuse Counseling for victim of child abuse
V61.29 Z62.898
Other specified problems related to
upbringing (e.g., Problem concerning
adopted or foster child)
V61.41 Z63.72 Alcoholism and drug addiction in family
V61.49 Z63.6 Dependent relative needing care at home (e.g., Care of sick or handicapped person in family or household)
V61.8 Z69.891 Other specified problems related to primary support group
V61.9 Z63.9 Problem related to primary support
group, unspecified
V62.4 Z60.3 Acculturation difficulty (e.g., Cultural deprivation, Social isolation or persecution)
V62.5 Z65.3 Problems related to other legal circumstances (e.g., Imprisonment)
V62.89 Z64.4 Other specified problems related to psychosocial circumstances (e.g., Life circumstance problems)
V62.9 Z65.9 Problem related to unspecified psychosocial circumstances
V65.49 Z71.89 Other specified counseling (Counseling for marital and partner problems, unspecified)
V69.9 Z72.9 Problems related to lifestyle, unspecified
V79.8 Z13.4 Encounter for screening for certain developmental disorders in childhood
V907.3 S14.3XXS
Injury of Brachial Plexus, Sequela Encounter
V91.12 O30.129
Triplet pregnancy with two or more monoamniotic fetuses, unspecified trimester
V91.19 O30.199
Triplet pregnancy, unable to determine number of placenta and number of amniotic sacs, unspecified trimester
top related