Disease #01158 (MRX-32 (mental retardation, X-linked, syndromic, type 32 (MRX-32)), OMIM:300886)

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Official abbreviation	MRX-32
Name	mental retardation, X-linked, syndromic, type 32 (MRX-32)
OMIM ID	300886
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLIC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A