Macular Corneal Dystrophy

Preferred Label : Macular Corneal Dystrophy;

NCIt definition : A stromal corneal dystrophy, with autosomal recessive inheritance, that is caused by lack of or abnormal keratan sulfate.;

Details

Origin ID

C34793;

UMLS CUI

C0024439;

Automatic exact mappings (from CISMeF team)
- Macular corneal dystrophy [ICD-11 More detail]
- Macular corneal dystrophy [ICD-9 code]
- corneal dystrophies, hereditary [MeSH Descriptor]
Currated CISMeF NLP mapping
- Macular corneal dystrophy [MedDRA LLT]
- Macular corneal dystrophy [ORDO Disease]
- Macular corneal dystrophy (disorder) [SNOMED CT concept]
- Macular dystrophy, corneal [OMIM Phenotype]
- Macular dystrophy, corneal type 1 [MeSH concept]
- macular corneal dystrophy [DO Concept]
- macular corneal dystrophy [Disease (Nov.)]
- macular corneal dystrophy [SNOMED Notion]
- macular dystrophy, corneal [MeSH concept]
- macular dystrophy, corneal type 1 [MeSH Supplementary Concept]
DO Cross reference
- macular corneal dystrophy [DO Concept]
Has associated anatomic sites
- Cornea [NCIt concept]
- Eye [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Macular corneal dystrophy [MedDRA LLT]
- Macular corneal dystrophy [ICD-9 code]
- Macular corneal dystrophy (disorder) [SNOMED CT concept]
- macular corneal dystrophy [DO Concept]
- macular corneal dystrophy [Disease (Nov.)]
- macular corneal dystrophy [SNOMED Notion]
- macular dystrophy, corneal [MeSH concept]
Validated automatic mappings to BTNT
- macular corneal dystrophy type 1 [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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