Disease #00037

Official abbreviation MC3DN-1
Name mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)]
OMIM ID 124000
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 2 genes BCS1L, UQCRC2
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00000269 - - - - - - - - - - - MC3DN-1 UQCRC2 UQCRC2 1 1 Noriko Miyake
00001829 - - - F yes Morocco - - 0 - - MC3DN-1 LYRM7 LYRM7 1 1 Daniele Ghezzi
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