Disease #02561 (MMDS1 (mitochondrial dysfunctions, multiple, syndrome, type 1), OMIM:605711)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS1
Name	mitochondrial dysfunctions, multiple, syndrome, type 1
OMIM ID	605711
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NFU1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-11-25 10:04:58 +01:00 (CET)

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