Disease #03705 (CTRCT38;CATC5 (cataract, type 38 (CTRCT-38, cataract, autosomal recessive congenital 5 (CATC-5))), OMIM:614691)

Official abbreviation	CTRCT38;CATC5
Name	cataract, type 38 (CTRCT-38, cataract, autosomal recessive congenital 5 (CATC-5))
OMIM ID	614691
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AGK
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD