Disease #00019 (Xp11.22 microduplication (microduplication syndrome, Xp11.22 (MRX17;MRX31)), OMIM:300705)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	Xp11.22 microduplication
Name	microduplication syndrome, Xp11.22 (MRX17;MRX31)
OMIM ID	300705
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HUWE1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-23 10:51:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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