Disease #05982 (MRT72 (intellectual developmental disorder, autosomal recessive, type 12 (MRT72)), OMIM:618665)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRT72
Name	intellectual developmental disorder, autosomal recessive, type 12 (MRT72)
OMIM ID	618665
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	METTL5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-28 08:07:11 +02:00 (CEST)
Date last edited	N/A

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