Disease #00253 (FRA12A (mental retardation, FRA12A type (FRA-12A)), OMIM:136630)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FRA12A
Name	mental retardation, FRA12A type (FRA-12A)
OMIM ID	136630
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 1 gene	DIP2B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-20 15:12:39 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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