OMOP Concept 4196109
Inherited optic neuropathy
StandardConditionSNOMED312942003Disorder
Maps from
0
Descendants
59
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Inherited optic neuropathy across source vocabularies.
- Inherited optic neuropathy (disorder)
- neuropatía óptica hereditaria
- neuropatía óptica hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Disorder of optic nerve
- 1Hereditary disorder of nervous system
- 1Hereditary disorder of the visual system
- 2Cranial nerve disorder
- 2Disorder of nervous system
- 2Disorder of visual pathways
- 2Hereditary disorder by system
- 2Visual system disorder
- 3Disorder of body system
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Eye / vision finding
- 3Finding of head region
- 3Hereditary disease
- 3Neuropathy
- 4Central nervous system finding
- 4Clinical finding
- 4Disease
- 4Genetic disease
- 4Head finding
Narrower concepts
(59)Included automatically when you query with descendants.
- 1Acro-oto-ocular syndrome
- 1Auditory neuropathy, optic atrophy syndrome
- 1Autosomal recessive isolated optic atrophy
- 1Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 1Behr syndrome
- 1CAMOS syndrome
- 1Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
- 1Colobomatous macrophthalmia with microcornea syndrome
- 1Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome
- 1Combined immunodeficiency with faciooculoskeletal anomalies syndrome
- 1COMMAD syndrome
- 1Familial cavitary optic disc anomaly
- 1GAPO syndrome
- 1Hereditary optic atrophy
- 1Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
- 1Multiple mitochondrial dysfunctions syndrome type 4
- 1Ocular anomalies, axonal neuropathy, developmental delay syndrome
- 1Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
- 1Optic nerve edema, splenomegaly syndrome
- 1PLAA-associated neurodevelopmental disorder
- 1Polymicrogyria with optic nerve hypoplasia
- 1Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome
- 1Severe X-linked intellectual disability Gustavson type
- 1Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome
- 1Wolfram syndrome
Showing 25 of 59. Retrieve the full set via the API.
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