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DO Term : mitochondrial complex III deficiency nuclear type 8 [DOID:0080117] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:615838,
  • 615838
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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