mitochondrial complex III deficiency nuclear type 8

mitochondrial complex III deficiency nuclear type 8

http://purl.obolibrary.org/obo/DOID_0080117

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://purl.obolibrary.org/obo/ECO_0007636 url:http://omim.org/entry/615838?search=615838&highlight=615838 ]

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This is just here as a test because I lose it

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MIM:615838

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disease_ontology

DOID:0080117

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mitochondrial complex III deficiency
disease has basis in some structural_variant