8 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: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:0080006 | bone development disease | A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage. |
DOID:1934 | dysostosis | A bone development disease that results in defective ossification of bone. |
DOID:0060379 | acrofacial dysostosis | A hetergeneous dysostosis that is characterized by digital dysplasia, downslanted palpebral fissures, deafness and developmental delay, has_material_basis_in mutation to the SF3B4 gene. |
13 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0060379 | DOID:0060353 |
is_a | DOID:1934 | DOID:0060379 |
is_a | DOID:4 | DOID:0060379 |
is_a | DOID:0080006 | DOID:0060379 |
is_a | DOID:65 | DOID:0060379 |
is_a | DOID:0080001 | DOID:0060379 |
is_a | DOID:17 | DOID:0060379 |
is_a | DOID:7 | DOID:0060379 |
is_a | DOID:0060379 | DOID:0060383 |
is_a | DOID:0060379 | DOID:0060384 |
is_a | DOID:0060379 | DOID:0060385 |
is_a | DOID:0060379 | DOID:0111571 |
is_a | DOID:0060379 | DOID:5768 |