Disease #05179 (MTCO1 (deficiency, cytochrome Coxidase subunit I (MTCO-1)), OMIM:516030)

Official abbreviation MTCO1
Name deficiency, cytochrome Coxidase subunit I (MTCO-1)
OMIM ID 516030
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MT-CO1
Associated tissues -
Disease features -
Remarks -
Date created 2016-09-13 15:57:13 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080796 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DLDD, MTCO1 Cytochrome c oxidase subunit I (OMIM:516030), Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) DLD, MT-CO1 DLD, MT-CO1 2 1 Daniel Trujillano
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