Disease #05952 (CAFDADD (cardiac, facial, and digital anomalies with developmental delay (CAFDADD)), OMIM:618164)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CAFDADD
Name	cardiac, facial, and digital anomalies with developmental delay (CAFDADD)
OMIM ID	618164
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRAF7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-06-29 15:39:26 +02:00 (CEST)
Date last edited	N/A

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