Disease #05679 (MRT57 (mental retardation, autosomal recessive, type 57 (MRT57)), OMIM:617188)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRT57
Name	mental retardation, autosomal recessive, type 57 (MRT57)
OMIM ID	617188
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MBOAT7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-12-29 13:08:00 +01:00 (CET)
Date last edited	N/A

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