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WormBase Tree Display for DO_term: DOID:0111501

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Name Class

DOID:0111501Namecombined oxidative phosphorylation deficiency 29
StatusValid
DefinitionA combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the TXN2 gene on chromosome 22q12.3.
SynonymExactCOXPD29
ParentIs_aDOID:0050737
DOID:0060286
DB_infoDatabaseOMIMdisease616811
Attribute_ofGene_by_orthologyWBGene00007099