Corneal dystrophy, endothelial, X-linked

Preferred Label : Corneal dystrophy, endothelial, X-linked;

Symbol : XECD;

CISMeF acronym : XECD;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Endothelial corneal dystrophy, X-linked;

Inheritance : X-linked dominant;

Prefixed ID : %300779;

Details

Origin ID

300779;

UMLS CUI

C2749049;

Automatic exact mappings (from CISMeF team)
- X-linked endothelial corneal dystrophy [ICD-11 More detail]
Currated CISMeF NLP mapping
- X-linked endothelial corneal dystrophy [DO Concept]
- X-linked endothelial corneal dystrophy [ORDO Disease]
- X-linked endothelial dystrophy of cornea (disorder) [SNOMED CT concept]
- corneal dystrophy, endothelial, X-Linked [MeSH concept]
- corneal dystrophy, endothelial, X-Linked [MeSH Supplementary Concept]
DO Cross reference
- X-linked endothelial corneal dystrophy [DO Concept]
HPO term(s)
- Band keratopathy [HPO term]
- Corneal dystrophy [HPO term]
- Corneal opacity [HPO term]
- X-linked dominant inheritance [HPO term]
ORDO concept(s)
- X-linked endothelial corneal dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- X-linked endothelial corneal dystrophy [ORDO Disease]
- X-linked endothelial corneal dystrophy [DO Concept]
- X-linked endothelial dystrophy of cornea (disorder) [SNOMED CT concept]
- corneal dystrophy, endothelial, X-Linked [MeSH Supplementary Concept]
- corneal dystrophy, endothelial, X-Linked [MeSH concept]

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