Disease #07103 (CAGS (Chopra-Amiel-Gordon syndrome), OMIM:619504)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CAGS
Name	Chopra-Amiel-Gordon syndrome
OMIM ID	619504
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ANKRD17
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-18 09:51:16 +02:00 (CEST)
Date last edited	N/A

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