Disease #01119 (MRX96 (mental retardation, X-linked, type 96 (MRX96)), OMIM:300802)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX96
Name	mental retardation, X-linked, type 96 (MRX96)
OMIM ID	300802
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SYP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-11 17:00:41 +02:00 (CEST)

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