9 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:535 | sleep disorder | A disease of mental health that involves disruption of sleep patterns. |
| DOID:0050628 | advanced sleep phase syndrome | A sleep disorder that involves an altered circadian rhythm resulting in falling asleep in early evening and awaking very early in the morning. |
| DOID:0110011 | advanced sleep phase syndrome 1 | An advanced sleep phase syndrome that has_material_basis_in heterozygous mutation in the PER2 gene on chromosome 2q37. |
8 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050628 | DOID:0110011 |
| is_a | DOID:0050739 | DOID:0110011 |
| is_a | DOID:150 | DOID:0110011 |
| is_a | DOID:0050177 | DOID:0110011 |
| is_a | DOID:535 | DOID:0110011 |
| is_a | DOID:4 | DOID:0110011 |
| is_a | DOID:0050736 | DOID:0110011 |
| is_a | DOID:630 | DOID:0110011 |
