10 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: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:150 | disease of mental health | A disease that involves a psychological or behavioral pattern generally associated with subjective distress or disability that occurs in an individual, and which are not a part of normal development or culture. |
| DOID:1561 | cognitive disorder | A disease of mental health that affects cognitive functions including memory processing, perception and problem solving. |
| DOID:5419 | schizophrenia | A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. |
| DOID:2468 | psychotic disorder | A cognitive disorder that involves abnormal thinking and perceptions resulting in a disconnection with reality. |
| DOID:0070088 | schizophrenia 12 | A schizophrenia that has_material_basis_in a mutation on chromosome 1p36.2. |
9 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:5419 | DOID:0070088 |
| is_a | DOID:0050736 | DOID:0070088 |
| is_a | DOID:630 | DOID:0070088 |
| is_a | DOID:1561 | DOID:0070088 |
| is_a | DOID:4 | DOID:0070088 |
| is_a | DOID:2468 | DOID:0070088 |
| is_a | DOID:0050739 | DOID:0070088 |
| is_a | DOID:150 | DOID:0070088 |
| is_a | DOID:0050177 | DOID:0070088 |
