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DO Term : Fuchs' endothelial dystrophy [DOID:11555] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision.

synonyms:
NCI:C84721,
OMIM:613270,
MESH:D005642,
610158,
OMIM:615523,
Fuchs' endothelial corneal dystrophy,
ORDO:98974,
OMIM:610158,
615523,
136800,
FCED,
613271,
613269,
613267,
OMIM:613268,
OMIM:613269,
UMLS_CUI:C0016781,
OMIM:613267,
OMIM:613271,
GARD:10018,
OMIM:136800,
613270,
Fuchs' corneal dystrophy,
SNOMEDCT_US_2023_03_01:16949007,
613268,
ICD10CM:H18.51

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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