macular dystrophy, corneal type 1

Preferred Label : macular dystrophy, corneal type 1;

MeSH synonym : macular corneal dystrophy type 1; corneal dystrophy, macular type; groenouw type II corneal dystrophy; macular dystrophy, corneal, 1; macular corneal dystrophy, type I; mcd; Mcdc1;

Détails

Origin ID

C537834;

UMLS CUI

C1636149;

Automatic exact mappings (from CISMeF team)
- Groenouw type II corneal dystrophy [PASCAL descriptor]
- Kaposi sarcoma, susceptibility to [OMIM Phenotype]
- Malonyl-coa decarboxylase [OMIM gene]
- Multicentric Castleman disease [ORDO Disease]
- Multiple carboxylase deficiency [ORDO Disease]
- carbohydrate sulfotransferase 6 [ORDO Gene]
- malonyl-CoA decarboxylase [ORDO Gene]
- mucin 1, cell surface associated [ORDO Gene]
- multicentric Castleman disease [DO Concept]
CISMeF manual mappings
- macular corneal dystrophy [SNOMED Notion]
Currated CISMeF NLP mapping
- Macular Corneal Dystrophy [NCIt concept]
- Macular corneal dystrophy [ORDO Disease]
- Macular corneal dystrophy [MedDRA LLT]
- Macular corneal dystrophy (disorder) [SNOMED CT concept]
- Macular corneal dystrophy Type I (disorder) [SNOMED CT concept]
- Macular dystrophy, corneal [OMIM Phenotype]
- macular corneal dystrophy [DO Concept]
- macular corneal dystrophy type 1 [Disease (Nov.)]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
Record concept(s)
- Macular dystrophy, corneal type 1 [MeSH concept]
See also inter- (CISMeF)
- Granular corneal dystrophy type I [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Macular corneal dystrophy Type I (disorder) [SNOMED CT concept]
- Macular dystrophy, corneal [OMIM Phenotype]
- macular corneal dystrophy type 1 [Disease (Nov.)]
Validated automatic mappings to NTBT
- macular corneal dystrophy [Disease (Nov.)]

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