Disease #04506 (MMDS3 (mitochondrial dysfunctions, multiple, syndrome, type 3), OMIM:615330)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS3
Name	mitochondrial dysfunctions, multiple, syndrome, type 3
OMIM ID	615330
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IBA57
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2024-11-25 10:02:06 +01:00 (CET)

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