Disease #05948 (MRT58 (mental retardation, autosomal recessive, type 58 (MRT58)), OMIM:617270)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRT58
Name	mental retardation, autosomal recessive, type 58 (MRT58)
OMIM ID	617270
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ELP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-06-14 19:14:04 +02:00 (CEST)
Date last edited	N/A

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