OMOP Concept 4181326
Hereditary disorder of the visual system
StandardConditionSNOMED363343008Disorder
Maps from
1
Descendants
517
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary disorder of the visual system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 363343008 | Hereditary disorder of the visual system | Non-standard |
Synonyms
Alternative names recorded for Hereditary disorder of the visual system across source vocabularies.
- Hereditary disorder of the visual system (disorder)
- trastorno hereditario del aparato visual
- trastorno hereditario del aparato visual (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(517)Included automatically when you query with descendants.
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- 1Acrorenoocular syndrome
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- 1Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 1Aicardi's syndrome
- 1Alacrima
- 1Albinotic fundus
- 1Aniridia and absent patella syndrome
- 1Aniridia and intellectual disability syndrome
- 1Aniridia, ptosis, intellectual disability, familial obesity syndrome
- 1Aniridia, renal agenesis, psychomotor retardation syndrome
- 1Anophthalmia plus syndrome
- 1Anterior maxillary protrusion, strabismus, intellectual disability syndrome
- 1Aplasia cutis congenita with epibulbar dermoid syndrome
- 1Aplasia cutis with myopia syndrome
- 1Aplasia of lacrimal and salivary gland
- 1Ataxia with tapetoretinal degeneration syndrome
- 1Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome
- 1Atrophia bulborum hereditaria
- 1Autosomal dominant cystoid macular edema
- 1Autosomal dominant keratitis
- 1Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
- 1Autosomal dominant neovascular inflammatory vitreoretinopathy
- 1Autosomal dominant progressive external ophthalmoplegia
- 1Autosomal dominant pterygium of conjunctiva
- 1Autosomal dominant rhegmatogenous retinal detachment
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
- 1Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
- 1Autosomal recessive chorioretinopathy and microcephaly syndrome
- 1Autosomal recessive dysgenesis of anterior segment of eye
- 1Autosomal recessive progressive external ophthalmoplegia
- 1Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
- 1Axenfeld anomaly
- 1Best vitelliform macular dystrophy
- 1Blepharophimosis, intellectual disability syndrome, Verloes type
- 1Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
- 1Blepharoptosis, myopia, ectopia lentis syndrome
- 1Blindness, scoliosis, arachnodactyly syndrome
- 1Brachydactyly, short stature, retinitis pigmentosa syndrome
- 1Bradyopsia
- 1Brittle cornea syndrome
- 1Cardiomyopathy with cataract and hip spine disease syndrome
- 1Cataract and microcornea syndrome
- 1Cataract, congenital heart disease, neural tube defect syndrome
- 1Cataract glaucoma syndrome
- 1Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
- 1Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
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