Disease #02207 (MRX99 (mental retardation, X-linked, type 99 (MRX99)), OMIM:300919)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX99
Name	mental retardation, X-linked, type 99 (MRX99)
OMIM ID	300919
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	USP9X
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-11 16:59:03 +02:00 (CEST)

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