Corneal dystrophy, fuchs endothelial, 5

Preferred Label : Corneal dystrophy, fuchs endothelial, 5;

Symbol : FECD5;

CISMeF acronym : FECD5;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Corneal dystrophy, fuchs endothelial, late-onset; Fcd3 locus;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of Fuchs corneal dystrophy, see FECD1 (136800).;

Prefixed ID : %613269;

Details

Origin ID

613269;

UMLS CUI

C2750449;

Currated CISMeF NLP mapping
- corneal dystrophy, fuchs endothelial, 5 [MeSH concept]
- corneal dystrophy, fuchs endothelial, 5 [MeSH Supplementary Concept]
DO Cross reference
- Fuchs' endothelial dystrophy [DO Concept]
ORDO concept(s)
- Fuchs endothelial corneal dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- corneal dystrophy, fuchs endothelial, 5 [MeSH Supplementary Concept]
- corneal dystrophy, fuchs endothelial, 5 [MeSH concept]
Validated automatic mappings to NTBT
- Fuchs endothelial corneal dystrophy [ORDO Disease]
- Fuchs' endothelial dystrophy [DO Concept]

Keyword's position in hierarchy(ies) :

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