Disease #05682 (VCRL2 (vertebral, cardiac, renal, and limb defects syndrome, type 2 (VCRL2)), OMIM:617661)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	VCRL2
Name	vertebral, cardiac, renal, and limb defects syndrome, type 2 (VCRL2)
OMIM ID	617661
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KYNU
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-01-06 15:55:01 +01:00 (CET)
Date last edited	N/A

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