Disease #01123 (MRX88 (mental retardation, X-linked, type 88 (MRX88)), OMIM:300852)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRX88
Name	mental retardation, X-linked, type 88 (MRX88)
OMIM ID	300852
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AGTR2
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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