18 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 involves errors in metabolic processes of building or degradation of molecules. |
| DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
| DOID:417 | autoimmune disease | An immune system disease that is an overactive immune response of the body against substances and tissues normally present in the body resulting from an abnormal functioning of the immune system that results in the production of antibodies or T cell directed against the host tissues. |
| DOID:612 | primary immunodeficiency disease | An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation. |
| DOID:0060005 | autoimmune disease of endocrine system | An autoimmune disease that is the abnormal functioning of the immune system resulting in production of antibodies or T cells against cells and/or tissues in the endocrine system. |
| DOID:28 | endocrine system disease | A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body. |
| DOID:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0050736 | autosomal dominant disease | An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
| DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| 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:9351 | diabetes mellitus | A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both. |
| DOID:2978 | carbohydrate metabolic disorder | An inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates. |
| DOID:4194 | glucose metabolism disease | A carbohydrate metabolic disorder that is characterized by blood glucose levels which cannot be maintained within the normal range. |
| DOID:9744 | type 1 diabetes mellitus | A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production. |
| DOID:0110741 | type 1 diabetes mellitus 2 | A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. |
17 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050736 | DOID:0110741 |
| is_a | DOID:9744 | DOID:0110741 |
| is_a | DOID:28 | DOID:0110741 |
| is_a | DOID:417 | DOID:0110741 |
| is_a | DOID:612 | DOID:0110741 |
| is_a | DOID:4 | DOID:0110741 |
| is_a | DOID:655 | DOID:0110741 |
| is_a | DOID:0014667 | DOID:0110741 |
| is_a | DOID:7 | DOID:0110741 |
| is_a | DOID:4194 | DOID:0110741 |
| is_a | DOID:9351 | DOID:0110741 |
| is_a | DOID:0060005 | DOID:0110741 |
| is_a | DOID:0050739 | DOID:0110741 |
| is_a | DOID:630 | DOID:0110741 |
| is_a | DOID:2978 | DOID:0110741 |
| is_a | DOID:0050177 | DOID:0110741 |
| is_a | DOID:2914 | DOID:0110741 |
