Disease #05661 (MRX107 (mental retardation, X-linked, type 107 (MRX107)), OMIM:301013)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX107
Name	mental retardation, X-linked, type 107 (MRX107)
OMIM ID	301013
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CXorf56
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-10-15 15:27:06 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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