Disease #00800 (MRT7 (mental retardation, autosomal recessive, type 7 (MRT7)), OMIM:611093)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRT7
Name	mental retardation, autosomal recessive, type 7 (MRT7)
OMIM ID	611093
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TUSC3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-10-15 09:38:50 +02:00 (CEST)

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