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

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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