Disease #02400 (CTRCT14;CZP3 (cataract, type 14), OMIM:601885)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CTRCT14;CZP3
Name	cataract, type 14
OMIM ID	601885
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GJA3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-03-17 16:13:09 +01:00 (CET)

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