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: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:0080005 | bone remodeling disease | A bone disease that results_in formation or resorption abnormalities located_in bone. |
| DOID:4254 | osteosclerosis | A bone remodeling disease that results_in abnormal elevated bone density or mass. |
| DOID:13533 | osteopetrosis | An osteosclerosis that has_material_basis_in lack of bone resorption which results_in abnormally hard and brittle bones. |
| DOID:0110938 | autosomal dominant osteopetrosis 2 | An osteopetrosis characterized by autosomal dominant inheritance of sclerosis predominantly involving the spine, the pelvis, and the skull base, bone fragility and dental abscesses that has_material_basis_in mutation in the CLCN7 gene on chromosome 16p13. |
13 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:13533 | DOID:0110938 |
| is_a | DOID:0060564 | DOID:0110938 |
| is_a | DOID:0050736 | DOID:0110938 |
| is_a | DOID:0050739 | DOID:0110938 |
| is_a | DOID:65 | DOID:0110938 |
| is_a | DOID:0080005 | DOID:0110938 |
| is_a | DOID:0050177 | DOID:0110938 |
| is_a | DOID:7 | DOID:0110938 |
| is_a | DOID:0080001 | DOID:0110938 |
| is_a | DOID:630 | DOID:0110938 |
| is_a | DOID:4254 | DOID:0110938 |
| is_a | DOID:4 | DOID:0110938 |
| is_a | DOID:17 | DOID:0110938 |
