Hereditary Retinal Dystrophy

Preferred Label : Hereditary Retinal Dystrophy;

NCIt definition : An inherited form of retinal dystrophy.;

Details

Origin ID

C35194;

UMLS CUI

C0154860;

Currated CISMeF NLP mapping
- Hereditary retinal dystrophies [ICD-9 code]
- Hereditary retinal dystrophies [MedDRA LLT]
- Hereditary retinal dystrophy [ICD-10 Sub-category]
- Hereditary retinal dystrophy [ICD-10 Sub-category (who)]
- Hereditary retinal dystrophy [MedDRA Preferred Term]
- Hereditary retinal dystrophy (disorder) [SNOMED CT concept]
- Hereditary retinal dystrophy, unspecified [ICD-9 code]
- Hereditary retinal dystrophy, unspecified [MedDRA LLT]
- Inherited retinal dystrophies [ICD-11 Category]
- hereditary retinal dystrophy [Disease (Nov.)]
- hereditary retinal dystrophy [DO Concept]
- hereditary retinal dystrophy, nos [SNOMED Notion]
DO Cross reference
- hereditary retinal dystrophy [DO Concept]
Has associated anatomic sites
- Eye [NCIt concept]
- Retina [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary retinal dystrophies [ICD-9 code]
- Hereditary retinal dystrophies [MedDRA LLT]
- Hereditary retinal dystrophy [ICD-10 Sub-category]
- Hereditary retinal dystrophy [ICD-10 Sub-category (who)]
- Hereditary retinal dystrophy [MedDRA Preferred Term]
- Hereditary retinal dystrophy (disorder) [SNOMED CT concept]
- Hereditary retinal dystrophy, unspecified [MedDRA LLT]
- Hereditary retinal dystrophy, unspecified [ICD-9 code]
- Inherited retinal dystrophies [ICD-11 Category]
- hereditary retinal dystrophy [DO Concept]
- hereditary retinal dystrophy [Disease (Nov.)]
- hereditary retinal dystrophy, nos [SNOMED Notion]
disease_has_finding
- Hereditary Lesion [NCIt concept]

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