Search Ontology:
Human Disease

mitochondrial complex III deficiency nuclear type 8

Term ID
DOID:0080117
Synonyms
Definition
A mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has_material_basis_in homozygous mutation in the LYRM7 gene on chromosome 5q23. http://omim.org/entry/615838?search=615838&highlight=615838
References
  • MIM:615838
Ontology
Human Disease   ( DOID:0080117 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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