Disease #05632 (MMDS5 (mitochondrial dysfunctions, multiple, syndrome, type 5), OMIM:617613)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS5
Name	mitochondrial dysfunctions, multiple, syndrome, type 5
OMIM ID	617613
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ISCA1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-07-28 12:46:00 +02:00 (CEST)
Date last edited	2024-11-25 10:00:13 +01:00 (CET)

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