Disease #07137 (MMDS9B (mitochondrial dysfunctions, multiple, syndrome, type 9B), OMIM:620887)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MMDS9B
Name	mitochondrial dysfunctions, multiple, syndrome, type 9B
OMIM ID	620887
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FDXR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-25 10:01:34 +01:00 (CET)
Date last edited	N/A

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