Disease #05560 (CTRCT46 (cataract, type 46, juvenile-onset (CTRCT-46)), OMIM:212500)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CTRCT46
Name	cataract, type 46, juvenile-onset (CTRCT-46)
OMIM ID	212500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LEMD2
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-02-12 09:12:36 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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