Disease #01116 (MRX89 (mental retardation, X-linked, type 89 (MRX89)), OMIM:300848)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX89
Name	mental retardation, X-linked, type 89 (MRX89)
OMIM ID	300848
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ZNF41
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-11 15:16:08 +02:00 (CEST)

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