WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111139 mitochondrial complex III deficiency Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III.

1 Ontology

Name
Disease Ontology

6 Parents

Identifier Name Description
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:0014667 disease of metabolism A disease that involves errors in metabolic processes of building or degradation of molecules.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:655 inherited metabolic disorder A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.
DOID:700 mitochondrial metabolism disease An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
DOID:0111139 mitochondrial complex III deficiency A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III.

14 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0111139 DOID:0060351
is_a DOID:0111139 DOID:0080111
is_a DOID:0111139 DOID:0080112
is_a DOID:0111139 DOID:0080113
is_a DOID:0111139 DOID:0080114
is_a DOID:0111139 DOID:0080115
is_a DOID:0111139 DOID:0080116
is_a DOID:0111139 DOID:0080117
is_a DOID:0111139 DOID:0080118
is_a DOID:700 DOID:0111139
is_a DOID:0014667 DOID:0111139
is_a DOID:4 DOID:0111139
is_a DOID:630 DOID:0111139
is_a DOID:655 DOID:0111139

0 Synonyms