Disease #05681 (VCRL1 (vertebral, cardiac, renal, and limb defects syndrome, type 1 (VCRL1)), OMIM:617660)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	VCRL1
Name	vertebral, cardiac, renal, and limb defects syndrome, type 1 (VCRL1)
OMIM ID	617660
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HAAO
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-01-06 15:54:12 +01:00 (CET)
Date last edited	N/A

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