Disease #03982 (MRT-38 (mental retardation, autosomal recessive, type 38 (MRT-38)), OMIM:615516)

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Official abbreviation	MRT-38
Name	mental retardation, autosomal recessive, type 38 (MRT-38)
OMIM ID	615516
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HERC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A