Disease #05737 (MRX106 (mental retardation, X-linked, type 106 (MRX106)), OMIM:300997)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX106
Name	mental retardation, X-linked, type 106 (MRX106)
OMIM ID	300997
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	OGT
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-11 15:06:15 +02:00 (CEST)
Date last edited	N/A

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