Disease #05905 (SHDRA (heart defects, structural, and renal anomalies syndrome (SHDRA)), OMIM:617478)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SHDRA
Name	heart defects, structural, and renal anomalies syndrome (SHDRA)
OMIM ID	617478
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C14orf101
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-03-13 18:48:20 +01:00 (CET)
Date last edited	N/A

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