Disease #06753 (MMDS6 (mitochondrial dysfunctions, multiple, syndrome, type 6), OMIM:617954)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS6
Name	mitochondrial dysfunctions, multiple, syndrome, type 6
OMIM ID	617954
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PMPCB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2024-11-25 10:06:53 +01:00 (CET)

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