ICD-9 Code ICD-10 Code Condition/Diagnosis 042 B20 Human … · 2020-02-16 · 270.2 E70.20 Disorder of tyrosine metabolism, unspecified 270.2 E70.21 Tyrosinemia, (Type I (Tyrosinosisa)

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

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

344.9 G83.9 Paralytic syndrome, unspecified

345.00 G40.309


epileptic syndromes, not intractable,

without status epilepticus

345.01 G40.319


epileptic syndromes, intractable,


345.5 G40.311


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




onset, not intractable, without status

epilepticus

345.50 G40.011


symptomatic epilepsy and epileptic

syndromes with complex partial

seizures, not intractable, without status

epilepticus







345.50 G40.119



syndromes with simple partial seizures,

intractable, without status epilepticus

345.50 G40.219




seizures, intractable, without status

epilepticus

345.50 G40.A19




not intractable, without status

epilepticus

345.51 G40.011




seizures, not intractable, with status

epilepticus

345.51 G40.019




seizures, intractable, with status

epilepticus

345.51 G40.101








not intractable, with status epilepticus

345.51 G40.111




onset, intractable, with status epilepticus

345.51 G40.119




onset, intractable, without status

epilepticus

345.51 G40.A11




intractable, with status epilepticus

345.60 G40.821

Other generalized epilepsy and epileptic

syndromes, not intractable, with status

epilepticus

345.60 G40.822


syndromes, not intractable, without

status epilepticus

345.61 G40.823


syndromes, intractable, with status

epilepticus




345.61 G40.824


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,


345.81 G40.B19 Juvenile myoclonic epilepsy, intractable,


345.90 G40.901 Epilepsy, unspecified, not intractable,


345.90 G40.909 Epilepsy, unspecified, not intractable,













345.91 G40.911 Epilepsy, unspecified, intractable, with

status epilepticus

345.91 G40.919 Epilepsy, unspecified, intractable,


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


retinal break, left eye

361.0 H33.003


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


362.24 H35.13


362.25 H35.14


362.26 H35.15


362.27 H35.16


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


cataract, left eye

366 H26.003


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


hearing loss, unilateral, right ear, with

unrestricted hearing on the contralateral

side

389.2

H90.72


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


nondisjunction)


nondisjunction)


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


nondisjunction)


nondisjunction)


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



765.21 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



765.23 P07.25 Extreme immaturity of newborn,

gestational age 26 completed weeks


765.24 P07.31 Preterm newborn, gestational age 28 completed weeks


765.25 P07.33 Preterm newborn, gestational age 30

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




772.2 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

Documents

ICD-9 Code ICD-10 Code Condition/Diagnosis 042 B20 Human … · 2020-02-16 · 270.2 E70.20 Disorder of tyrosine metabolism, unspecified 270.2 E70.21 Tyrosinemia, (Type I (Tyrosinosisa)