Disease #01158 (MRXS32 (mental retardation, X-linked, syndromic, type 32 (MRX32)), OMIM:300886)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRXS32
Name	mental retardation, X-linked, syndromic, type 32 (MRX32)
OMIM ID	300886
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLIC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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