14 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:0060564 | spinal disease | A bone disease that is located_in the spine. |
| DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
| DOID:0080001 | bone disease | A connective tissue disease that affects the structure or development of bone or causes an impairment of normal bone function. |
| DOID:65 | connective tissue disease | A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage. |
| DOID:225 | syndrome | A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality. |
| 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:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |
| DOID:0080589 | Klippel-Feil syndrome 1 | A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22. |
| DOID:10426 | Klippel-Feil syndrome | A physical disorder that is characterized by abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra. |
13 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050736 | DOID:0080589 |
| is_a | DOID:10426 | DOID:0080589 |
| is_a | DOID:0050739 | DOID:0080589 |
| is_a | DOID:0080015 | DOID:0080589 |
| is_a | DOID:65 | DOID:0080589 |
| is_a | DOID:0050177 | DOID:0080589 |
| is_a | DOID:0060564 | DOID:0080589 |
| is_a | DOID:4 | DOID:0080589 |
| is_a | DOID:630 | DOID:0080589 |
| is_a | DOID:0080001 | DOID:0080589 |
| is_a | DOID:17 | DOID:0080589 |
| is_a | DOID:225 | DOID:0080589 |
| is_a | DOID:7 | DOID:0080589 |
