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 |