Disease #07138 (MMDS7 (mitochondrial dysfunctions, multiple, syndrome, type 7), OMIM:620423)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS7
Name	mitochondrial dysfunctions, multiple, syndrome, type 7
OMIM ID	620423
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GCSH
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-25 10:13:05 +01:00 (CET)
Date last edited	N/A

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