Disease #01093 (MRT-1 (mental retardation, autosomal recessive, type 1 (MRT-1)), OMIM:249500)

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Official abbreviation	MRT-1
Name	mental retardation, autosomal recessive, type 1 (MRT-1)
OMIM ID	249500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRSS12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A