Disease #04094 (MC3DN7 (mitochondrial complex III deficiency, nuclear type 7 (MC3DN-7)), OMIM:615824)

Official abbreviation MC3DN7
Name mitochondrial complex III deficiency, nuclear type 7 (MC3DN-7)
OMIM ID 615824
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 MNF1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00361897 - - - - - - - - - - - MC3DN7 Neuroregression and MRI brain showing leukoencephalopathy - NDUFV2 1 1 Anju Shukla
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