Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dislocation of arytenoid cartilage (disorder) |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Perichondritis of larynx |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Chondroradionecrosis of larynx |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Calcification of laryngeal cartilage |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Congenital abnormal fusion of centrum cartilage of sacral vertebra |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Congenital abnormal fusion of centrum cartilage of lumbar vertebra (disorder) |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of sacral vertebra |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of lumbar vertebra |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Congenital abnormal fusion of centrum cartilage of thoracic vertebra |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of thoracic vertebra |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Degeneration of cervical intervertebral disc co-occurrent with osteophyte of cervical vertebra (disorder) |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Degeneration of thoracic intervertebral disc co-occurrent with osteophyte (disorder) |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Degeneration of lumbar intervertebral disc co-occurrent with osteophyte of lumbar vertebra (disorder) |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome is a rare, genetic primary bone dysplasia disorder characterized by disproportionate short stature with shortening of upper and lower limbs, short and broad fingers with short hands, narrowed chest with rib abnormalities and pectus excavatum, abnormal chondral calcifications (including larynx, trachea and costal cartilages) and facial dysmorphism (frontal bossing, hypertelorism, prominent eyes, short flat nose, wide nostrils, high-arched palate, long philtrum). Platyspondyly (especially of cervical spine) and abnormal epiphyses and metaphyses are observed on radiography. Atlantoaxial instability causing spinal compression and recurrent respiratory disease are potential complications that may result lethal. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Dysplasia epiphysealis hemimelica |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
McCune Albright syndrome (disorder) |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Multiple congenital exostosis |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
A rare primary bone dysplasia characterized by Perthes-like pelvic anomalies (premature closure of the capital femoral epiphyses and widened femoral necks with flattened femoral heads), arthralgias of hips and knees, and occurrence of enchondromata and ecchondromata. There have been no further descriptions in the literature since 1971. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
pseudochondroplasie |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Enchondromatosis |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
An association reported in a single kindred characterized by the variable presence of the following features: anetodermia (macular atrophy of the skin), multiple exostoses, and brachydactyly type E. There have been no further descriptions in the literature since 1985. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Polyostotic fibrous dysplasia of bone |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Osteoglophonic dysplasia |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Metachondromatosis |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Carpotarsal osteochondromatosis is a very rare primary bone dysplasia disorder with characteristics of abnormal bone proliferation and osteochondromas in the upper and lower limbs. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Genochondromatosis type 2 is a rare genetic bone development disorder characterized by normal clavicles and symmetrical, generalized metaphyseal enchondromas, particularly in the distal femur, proximal humerus, and bones of the wrists, hands, and feet. Lesions regress later in life with growth cartilage obliteration. Clinical examination is normal and the course of the disease is benign. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
A rare primary bone dysplasia characterized by severe intrauterine and postnatal growth retardation and short stature in association with craniofacial dysmorphism (such as large forehead, triangular face, low-set ears, and micro-retrognathism) and osteochondrodysplastic lesions. Radiographic findings include epiphyseal maturation delay, abnormal metaphyses, a narrow thorax, small pelvis, and short and broad metacarpal bones and phalanges. There have been no further descriptions in the literature since 1996. |
Is a |
True |
Osteochondropathy |
Inferred relationship |
Some |
|
Fibrous dysplasia |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|
Closed fracture of triradiate cartilage and epiphysis of acetabulum (disorder) |
Is a |
False |
Osteochondropathy |
Inferred relationship |
Some |
|