Disease #00037 (MC3DN1 (mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)]), OMIM:124000)

Official abbreviation MC3DN1
Name mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)]
OMIM ID 124000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene BCS1L
Associated tissues -
Disease features -
Remarks -
Date created 2012-08-30 16:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00001829 patient PubMed: Invernizzi 2013 - F yes Morocco - - - - - MC3DN1 - LYRM7 LYRM7 1 1 Daniele Ghezzi
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