|
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:0060158
|
acquired metabolic disease
|
A disease of metabolism that has_material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption. |
|
DOID:5113
|
nutritional deficiency disease
|
A nutrition disease that is characterized by deficiency of a nutritional element, such as a vitamin, mineral, carbohydrate, protein, fat, or general energy content. |
|
DOID:374
|
nutrition disease
|
An acquired metabolic disease that is characterized by an insufficient intake of food or of certain nutrients, by an inability of the body to absorb and use nutrients, or by overconsumption of certain foods. |
|
DOID:74
|
hematopoietic system disease
|
A disease of anatomical entity that has_material_basis_in hematopoietic cells. |
|
DOID:2355
|
anemia
|
A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells. |
|
DOID:8455
|
pyridoxine deficiency anemia
|
A nutritional deficiency disease that is characterized by normocytic anemia associated with deficiency of pyridoxine (vitamin B6), and has_material_basis_in decreased intake, malabsorption, increased clearance or breakdown, and certain medications (eg isoniazid). |
