9 Parents
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
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 involving errors in metabolic processes of building or degradation of molecules. |
DOID:37 | skin disease | An integumentary system disease that is located_in skin. |
DOID:16 | integumentary system disease | A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages. |
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:13268 | porphyria | An inherited metabolic disorder that involves certain enzymes in the heme bio-synthetic pathway resulting in the overproduction and accumulation of the porphyrins. |
DOID:13271 | cutaneous porphyria |
8 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:13268 | DOID:13271 |
is_a | DOID:37 | DOID:13271 |
is_a | DOID:630 | DOID:13271 |
is_a | DOID:7 | DOID:13271 |
is_a | DOID:0014667 | DOID:13271 |
is_a | DOID:655 | DOID:13271 |
is_a | DOID:4 | DOID:13271 |
is_a | DOID:16 | DOID:13271 |