Disease #05882 (VCRL3 (vertebral, cardiac, renal, and limb defects syndrome, type 3 (VCRL3)), OMIM:618845)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	VCRL3
Name	vertebral, cardiac, renal, and limb defects syndrome, type 3 (VCRL3)
OMIM ID	618845
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NADSYN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-12-02 09:14:02 +01:00 (CET)
Date last edited	N/A

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