H35.50
BillableUnspecified hereditary retinal dystrophy
Unspecified hereditary retinal dystrophy
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- dystrophies primarily involving Bruch's membrane (H31.1-)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- diabetes mellitus related eye conditions (E09.3-, E10.3-, E11.3-, E13.3-)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury (trauma) of eye and orbit (S05.-)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- syphilis related eye disorders (A50.01, A50.3-, A51.43, A52.71)
- diabetic retinal disorders (E08.311-E08.359, E09.311-E09.359, E10.311-E10.359, E11.311-E11.359, E13.311-E13.359)
Also Known As / Clinical Terms
SNOMED CT
- Congenital anomaly of macula4041005
- Bilateral paralysis6481005
- Diplegia6481005
- Optic atrophy associated with retinal dystrophy19448008
- Congenital hypoplasia of penis34911001
- Hypoplasia of penis34911001
- Micropenis34911001
- Hereditary retinal dystrophy41799005
- Choreoathetosis43105007
- AVP-D - arginine vasopressin deficiency45369008
- Arginine vasopressin deficiency45369008
- Central diabetes insipidus45369008
- Cranial diabetes insipidus45369008
- Diabetes insipidus - pituitary45369008
- Neurogenic diabetes insipidus45369008
- Neurohypophyseal diabetes insipidus45369008
- Pituitary diabetes insipidus45369008
- Vasopressin deficiency45369008
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Familial juvenile macular degeneration syndrome70099003
- Stargardt disease70099003
- Stargardt's disease70099003
- Spastic paralysis78403003
- Muscle weakness of all four limbs91327001
- Quadriparesis91327001
- Tetraparesis91327001
- Retinal dystrophy in cerebroretinal lipidosis192788009
- Hereditary retinal dystrophies in lipidoses193400007
- CRB - Congenital retinal blindness193413001
- Congenital retinal blindness193413001
- Leber amaurosis193413001
- Leber congenital amaurosis193413001
- Leber's amaurosis193413001
- Retinal flecking247138002
- Android fat distribution248311001
- Central obesity248311001
- Centripetal obesity248311001
- Fat body with thin limbs248311001
- Obesity of face and trunk, sparing limbs248311001
- Truncal obesity248311001
- Immuno-osseous dysplasia254067002
- Spastic diplegia281411007
- Spastic quadriparesis298282001
- Spastic tetraparesis298282001
- Cone dystrophy312917007
- North Carolina macular dystrophy312925009
- Rod dystrophy313003009
- Retinal dystrophy314407005
- Cerebellar hypoplasia and tapetoretinal degeneration715436007
- Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration715436007
- Retinitis punctata albescens715562001
- Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome715628009
- MORM (mental retardation, truncal obesity, retinal dystrophy, micropenis) syndrome715628009
- MORM syndrome715628009
- Mental retardation, truncal obesity, retinal dystrophy and micropenis syndrome715628009
- Bothnia retinal dystrophy715647007
- Vasterbotten dystrophy715647007
- SECORD - Severe early childhood onset retinal dystrophy716663009
- Severe early childhood onset retinal dystrophy716663009
- Nanophthalmia716775009
- Autosomal dominant late-onset retinal degeneration719431007
- Late-onset retinal degeneration719431007
- Cone dystrophy with supernormal rod electroretinogram719455002
- Cone dystrophy with supernormal rod response719455002
- Benign concentric annular macular dystrophy719520001
- EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome720856002
- EEM syndrome720856002
- Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome720856002
- Oligocone syndrome722066001
- Oligocone trichromacy722066001
- HJMD (hypotrichosis, juvenile macular degeneration) syndrome723364003
- Hypotrichosis with juvenile macular degeneration syndrome723364003
- Mackay Shek Carr syndrome723503006
- Retinal degeneration, nanophthalmos, glaucoma syndrome723503006
- Autosomal recessive bestrophinopathy723828008
- Retinopathy Burgess Black type723828008
- RHE (retinohepatoendocrinologic) syndrome724000006
- RHE syndrome724000006
- Retinohepatoendocrinologic syndrome724000006
- Aland Islands eye disease725168006
- Forsius Eriksson syndrome725168006
- Forsius Eriksson type ocular albinism725168006
- X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency732246009
- X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome732246009
- Ausems Wittebol Post Hennekam syndrome732247000
- Cleft lip retinopathy syndrome732247000
- Bonnemann Meinecke Reich syndrome733049004
- Encephalopathy, intracerebral calcification, retinal degeneration syndrome733049004
- Fundus albipunctatus764939004
- Fleck retina of Kandori765191009
- Kandori fleck retina syndrome765191009
- Familial benign flecked retina770434009
- OCMD - occult macular dystrophy770667002
- OMD - occult macular dystrophy770667002
- Occult macular dystrophy770667002
- MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome771342004
- MRCS syndrome771342004
- Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome771342004
- Roifman syndrome773404000
- Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome773404000
- Progressive retinal dystrophy due to retinol transport defect773576000
- Retinol dystrophy, iris coloboma, comedogenic acne syndrome773576000
- Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome773583007
- Aphonia, deafness, retinal dystrophy, duplicated halluces, intellectual disability syndrome773583007
- Aphonia, hearing loss, retinal dystrophy, duplicated halluces, intellectual disability syndrome773583007
- Retinal dystrophy with inner nuclear layer and ganglion cell anomalies774152007
- Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies774152007
- Infantile cerebellar and retinal degeneration782822006
- Ataxia with tapetoretinal degeneration syndrome783203003
- Congenital hypoplasia of external genitalia1144390001
- Congenital hypoplasia of male external genitalia1144863004
- Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome1172636006
- Hunter Jurenka Thompson syndrome1208341008
- ORC (oculo-renal-cerebellar) syndrome1208341008
- Oculorenocerebellar syndrome1208341008
- Severe oculo-renal-cerebellar syndrome1208341008
- Liberfarb syndrome1284851009
- Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome1284851009
- Hereditary AVP (arginine vasopressin)-related polyuria1296911007
- Hereditary arginine vasopressin-related polyuria1296911007
- Hereditary vasopressin-related polyuria1296911007
- SHILCA syndrome1356736002
- Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome1356736002
- Bilateral weakness of legs691011000124106
- Weakness of bilateral lower extremities691011000124106
- Weakness of bilateral lower limb691011000124106
- Weakness of both legs691011000124106
- Weakness of both lower extremities691011000124106
- Weakness of both lower limbs691011000124106
- Congenital coloboma of bilateral irides15665721000119102
- Congenital coloboma of both irises15665721000119102
- Congenital coloboma of iris of left eye15665761000119107
- Congenital coloboma of iris of right eye15665681000119108
- Paresis of left lower extremity16018391000119104
- Paresis of left lower limb16018391000119104
- Paresis of right lower extremity16018431000119109
- Paresis of right lower limb16018431000119109
- Progressive chorea27751000119104
- Weakness of left leg570941000124100
- Weakness of left lower limb570941000124100
- Weakness of left upper limb570921000124107
- weakness of left arm570921000124107
- Weakness of right arm570961000124101
- Weakness of right upper limb570961000124101
- Weakness of right leg570971000124108
- Weakness of right lower limb570971000124108
Frequently Asked Questions
What is the ICD-10 code for unspecified hereditary retinal dystrophy?
The ICD-10-CM code for unspecified hereditary retinal dystrophy is H35.50. The full clinical description is "Unspecified hereditary retinal dystrophy". H35.50 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H35.50 mean?
ICD-10-CM code H35.50 represents "Unspecified hereditary retinal dystrophy". It is classified under Chapter 7: Diseases of the Eye and Adnexa and is a billable/specific code that can be used on a claim.
Is H35.50 a billable code?
Yes, H35.50 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H35.50 in?
H35.50 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What codes cannot be used with H35.50?
H35.50 has Excludes1 notes indicating codes that cannot be used together with it, including: dystrophies primarily involving Bruch's membrane (H31.1-).
What SNOMED CT codes does H35.50 map to?
H35.50 maps to 72 SNOMED CT concepts: 45369008, 725168006, 248311001, 254067002, 773583007, and 67 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H35.50?
H35.50 is linked to 1 UMLS Concept Unique Identifier: C0154860. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.