Disease #05059 (CTRCT43 (cataract?, type 43 (CTRCT-43)), OMIM:616279)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	CTRCT43
Name	cataract?, type 43 (CTRCT-43)
OMIM ID	616279
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UNC45B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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