Disease #04572 (MRX-13 (mental retardation, X-linked, syndromic, type 13 (MRX-13)), OMIM:300055)

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Official abbreviation	MRX-13
Name	mental retardation, X-linked, syndromic, type 13 (MRX-13)
OMIM ID	300055
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MECP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	N/A