Disease #04506 (MMDS-3 (mitochondrial dysfunctions, multiple?, syndrome, type 3 (MMDS-3)), OMIM:615330)

Official abbreviation MMDS-3
Name mitochondrial dysfunctions, multiple?, syndrome, type 3 (MMDS-3)
OMIM ID 615330
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene IBA57
Associated tissues -
Disease features -
Remarks -