8 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: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:11156 | anhidrosis | A hypohidrosis that is characterized by the inability to sweat and has_symptom hyperthermia and dry skin. |
DOID:0060603 | isolated anhidrosis with normal sweat glands | An anhidrosis that has_material_basis_in homozygous mutation in the ITPR2 gene on chromosome 12p11. |
DOID:1383 | sweat gland disease | A skin disease located_in the sweat glands. |
DOID:11155 | hypohidrosis | A sweat gland disease that is characterized by reduced ability to sweat, has_symptom hyperthermia and dry skin of affected areas, and has_material_basis_in trauma to the sweat glands. |
7 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:11156 | DOID:0060603 |
is_a | DOID:7 | DOID:0060603 |
is_a | DOID:1383 | DOID:0060603 |
is_a | DOID:16 | DOID:0060603 |
is_a | DOID:11155 | DOID:0060603 |
is_a | DOID:4 | DOID:0060603 |
is_a | DOID:37 | DOID:0060603 |