Disease #06992 (IDMYS (intellectual disability and myopathy syndrome), OMIM:619719)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	IDMYS
Name	intellectual disability and myopathy syndrome
OMIM ID	619719
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCC9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-01-03 13:23:46 +01:00 (CET)
Date last edited	N/A

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