H47.22
BillableHereditary optic atrophy
Hereditary optic atrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Leber's optic atrophy
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)
Also Known As / Clinical Terms
SNOMED CT
- Autosomal dominant optic atrophy2065009
- Dominant hereditary optic atrophy2065009
- Pelger-Huet cell15111002
- Pelger-Huët cell15111002
- Hereditary optic atrophy26360005
- Genetic anomaly of leucocyte47986005
- Genetic anomaly of leukocyte47986005
- Genetic leucocyte disorder47986005
- Genetic leukocyte disorder47986005
- LHON - Leber hereditary optic neuropathy58610003
- LHON - Leber's hereditary optic neuropathy58610003
- Leber hereditary optic neuropathy58610003
- Leber optic atrophy58610003
- Leber's optic atrophy58610003
- Axonal neuropathy60703000
- DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome70694009
- DIDMOAD syndrome70694009
- Marquardt-Loriaux syndrome70694009
- Wolfram syndrome70694009
- Pelger Huet anomaly85559002
- Pelger-Huet anomaly85559002
- Pelger-Huët anomaly85559002
- Optic nerve finding106152006
- Second cranial nerve finding106152006
- False anodontia109440005
- HMSN VI128203003
- Hereditary motor and sensory neuropathy type VI128203003
- Hereditary motor and sensory neuropathy with optic atrophy128203003
- Hereditary motor-sensory neuropathy with optic atrophy128203003
- Hereditary motor-sensory neuropathy, type VI128203003
- Hereditary sensory and motor neuropathy, type VI128203003
- Tooth absent234948008
- Tooth missing234948008
- Generalised dystonia425492002
- Generalized dystonia425492002
- ADOA (autosomal dominant optic atrophy) plus715374003
- Autosomal dominant optic atrophy plus syndrome715374003
- Autosomal dominant optic atrophy Kjer type717336005
- Autosomal dominant optic atrophy classic form717336005
- Kjer optic atrophy717336005
- Optic atrophy type 1717336005
- Autosomal dominant optic atrophy and peripheral neuropathy syndrome717975006
- Leber plus disease719430008
- Autosomal dominant optic atrophy and cataract719517009
- Autosomal dominant optic atrophy type 3719517009
- CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome720634003
- Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome720634003
- Early-onset X-linked optic atrophy721200000
- Non-Leber type optic atrophy with early-onset721200000
- Optic atrophy type 2721200000
- GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome721843003
- GAPO syndrome721843003
- Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome721843003
- Severe X-linked intellectual disability Gustavson type722213009
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome725139005
- Spastic paraplegia, optic atrophy, neuropathy syndrome725139005
- CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome726031001
- CAMOS syndrome726031001
- Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome726031001
- SCAR5 - spinocerebellar ataxia autosomal recessive 5726031001
- BBSOAS - Bosch Boonstra Schaaf optic atrophy syndrome770723007
- Bosch Boonstra Schaaf optic atrophy syndrome770723007
- Optic atrophy, intellectual disability syndrome770723007
- Autosomal recessive optic atrophy OPA7 (optic atrophy type 7)783065004
- Autosomal recessive optic atrophy OPA7 type783065004
- Autosomal recessive optic atrophy type 7783065004
- Autosomal recessive spastic ataxia type 4784347002
- Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome784347002
- SPAX 4 - autosomal recessive spastic ataxia type 4784347002
- SPOAN and SPOAN-related disorder789674008
- Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder789674008
- Childhood-onset autosomal dominant optic atrophy838307002
- Autosomal recessive optic atrophy type 6838345001
- Diffuse atrophy of cerebral structure1144427006
- Diffuse atrophy of cerebrum1144427006
- Global brain atrophy1144430004
- Autosomal recessive bilateral optic atrophy1156823006
- Absence of teeth1162783002
- Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome1172593006
- Autosomal recessive isolated optic atrophy1197151003
- Autosomal recessive non-syndromic optic atrophy1197151003
- Auditory neuropathy, optic atrophy syndrome1222649004
- Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome1222655009
- X-linked optic atrophy1231634003
- Autosomal recessive childhood-onset dystonia DYT29 type1236805005
- Childhood-onset generalised dystonia, optic atrophy syndrome1236805005
- Childhood-onset generalized dystonia, optic atrophy syndrome1236805005
- DYT29 - dystonia 291236805005
- MEPAN syndrome1236805005
- Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome1236805005
- SOPH (short stature, optic nerve atrophy, Pelger-Huët anomaly) syndrome1237618009
- Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome1237618009
- ANOAC (axonal neuropathy, optic atrophy, cognitive deficit) syndrome1260129000
- Axonal neuropathy, optic atrophy, cognitive deficit syndrome1260129000
- Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome1260129000
- WFS1 - Wolfram syndrome-11285518004
- Wolfram syndrome type 11285518004
- Wolfram syndrome type I1285518004
- WFS2 - Wolfram syndrome-21285519007
- Wolfram syndrome type 21285519007
- Wolfram syndrome type II1285519007
- Bilateral optic atrophy of eyes15632891000119109
- Optic atrophy of bilateral eyes15632891000119109
- Optic atrophy of both eyes15632891000119109
- Bilateral primary optic atrophy344271000119107
- Primary optic atrophy of bilateral eyes344271000119107
- Primary optic atrophy of both eyes344271000119107
- Hereditary bilateral optic atrophy15699081000119101
- Hereditary left optic atrophy15699161000119109
- Hereditary right optic atrophy15699121000119104
- Left primary optic atrophy338501000119109
- Primary optic atrophy of left eye338501000119109
- Primary optic atrophy of right eye332891000119102
- Right primary optic atrophy332891000119102
UMLS
- Atrophies, Hereditary OpticC0029125
- Atrophy, Hereditary OpticC0029125
- Hereditary Optic AtrophiesC0029125
- Hereditary Optic AtrophyC0029125
- Hereditary optic atrophyC0029125
- Hereditary optic atrophy (disorder)C0029125
- Optic Atrophies, HereditaryC0029125
- Optic Atrophy, HereditaryC0029125
- atrophy hereditary opticC0029125
- hereditary optic atrophiesC0029125
- Disease, Leber'sC0917796
- Diseases, Leber'sC0917796
- Hereditary Optic NeuroretinopathiesC0917796
- Hereditary Optic NeuroretinopathyC0917796
- Hereditary optic neuroretinopathyC0917796
- LEBER HEREDITARY OPTIC NEUROPATHYC0917796
- LEBER OPTIC ATROPHYC0917796
- LHONC0917796
- LHON - Leber hereditary optic neuropathyC0917796
- LHON - Leber's hereditary optic neuropathyC0917796
- Leber DiseaseC0917796
- Leber Hereditary Optic AtrophyC0917796
- Leber Hereditary Optic NeuropathyC0917796
- Leber Optic AtrophyC0917796
- Leber Optic Atrophy and DystoniaC0917796
- Leber Optic NeuropathyC0917796
- Leber hereditary optic atrophyC0917796
- Leber hereditary optic neuropathyC0917796
- Leber optic atrophyC0917796
- Leber optic atrophy featuresC0917796
- Leber optic degenerationC0917796
- Leber's DiseaseC0917796
- Leber's DiseasesC0917796
- Leber's Hereditary Optic AtrophyC0917796
- Leber's Hereditary Optic NeuropathyC0917796
- Leber's Optic AtrophyC0917796
- Leber's Optic NeuropathyC0917796
- Leber's diseaseC0917796
- Leber's hereditary optic atrophy neuropathyC0917796
- Leber's hereditary optic neuropathyC0917796
- Leber's optic atrophyC0917796
- Leber's optic atrophy (disorder)C0917796
- Leber's optic neuropathyC0917796
- Lebers DiseaseC0917796
- Lebers Optic NeuropathyC0917796
- Neuropathy, Leber's OpticC0917796
- Neuroretinopathies, Hereditary OpticC0917796
- Neuroretinopathy, Hereditary OpticC0917796
- Optic Atrophy, Hereditary, LeberC0917796
- Optic Atrophy, LeberC0917796
- Optic Atrophy, Leber TypeC0917796
- Optic Atrophy, Leber, HereditaryC0917796
- Optic Neuropathy, Leber'sC0917796
- Optic Neuroretinopathies, HereditaryC0917796
- Optic Neuroretinopathy, HereditaryC0917796
- leber optic atrophyC0917796
- leber's optic atrophyC0917796
Frequently Asked Questions
What is the ICD-10 code for hereditary optic atrophy?
The ICD-10-CM code for hereditary optic atrophy is H47.22. The full clinical description is "Hereditary optic atrophy". H47.22 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H47.22 mean?
ICD-10-CM code H47.22 represents "Hereditary optic atrophy". 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 H47.22 a billable code?
Yes, H47.22 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H47.22 in?
H47.22 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What SNOMED CT codes does H47.22 map to?
H47.22 maps to 52 SNOMED CT concepts: 715374003, 1260129000, 1162783002, 1222649004, 2065009, and 47 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H47.22?
H47.22 is linked to 2 UMLS Concept Unique Identifiers: C0029125, C0917796. 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.