Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024

Preferred Name	KERATITIS, HEREDITARY
Synonyms
ID	http://purl.bioontology.org/ontology/OMIM/148190
cui	C1835698
Gene Locus	11p13
Gene Symbol	FVH1 MGDA AN2 ASGD5 PAX6
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	148190
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	KERATITIS, HEREDITARY
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/C537022	MESH	CUI
http://purl.bioontology.org/ontology/SCTSPA/715339004	SCTSPA	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/715339004	SNOMEDCT	CUI
http://purl.obolibrary.org/obo/OMIM_148190	CCO	LOOM
http://purl.bioontology.org/ontology/MESH/C537022	MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537022	RH-MESH	LOOM
http://identifiers.org/omim/148190	REXO	LOOM
http://identifiers.org/omim/148190	GEXO	LOOM
http://identifiers.org/omim/148190	RETO	LOOM