Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/610158 http://purl.bioontology.org/ontology/OMIM/610158
Preferred Name	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
Synonyms	FCD1 LOCUS CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET FECD2
Type	http://www.w3.org/2002/07/owl#Class

altLabel	FCD1 LOCUS CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET FECD2
prefLabel	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
Gene Symbol	FECD2 FCD1
Scope Statement	Greater expression in females [MISCELLANEOUS] Ratio female to male, 19:10 in index family [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU024206 http://purl.bioontology.org/ontology/OMIM/MTHU024207 http://purl.bioontology.org/ontology/OMIM/MTHU024204 http://purl.bioontology.org/ontology/OMIM/MTHU024203 http://purl.bioontology.org/ontology/OMIM/MTHU029976 http://purl.bioontology.org/ontology/OMIM/MTHU024205 See more See less
tui	T047
Gene Locus	13pter-q12.13
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	610158
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C1857800
OMIM Entry Type	5
OMIM MimType Value	perc

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