Disease #06942 (MRT76 (intellectual developmental disorder, autosomal recessive, type 76), OMIM:619931)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRT76
Name	intellectual developmental disorder, autosomal recessive, type 76
OMIM ID	619931
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRIA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-06-30 19:42:24 +02:00 (CEST)
Date last edited	N/A

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