Disease #06860 (MC1DN12 (Mi complex I deficiency, nuclear type 12), OMIM:301020)

Official abbreviation MC1DN12
Name Mi complex I deficiency, nuclear type 12
OMIM ID 301020
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NDUFA1
Associated tissues -
Disease features -
Remarks -

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