loading...| Preferred Name |
Osteoarthropathy, Primary Hypertrophic [Disease/Finding] |
|
| Synonyms |
Idiopathic Hypertrophic Osteoarthropathy |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002245 |
|
| altLabel |
Idiopathic Hypertrophic Osteoarthropathy Pachydermoperiostosis Touraine-Solente-Gole Syndrome Osteoarthropathy, Primary Hypertrophic Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive Pachydermoperiostosis, Autosomal Recessive |
|
| cui |
C0029411 |
|
| MESH DEFINITION |
A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists. |
|
| MESH DUI |
D010004 |
|
| MeSH name |
Osteoarthropathy, Primary Hypertrophic |
|
| MESH UI |
M0015511 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002245 |
|
| NUI |
N0000002245 |
|
| prefLabel |
Osteoarthropathy, Primary Hypertrophic [Disease/Finding] |
|
| SNOMED CID |
223726008 88220006 |
|
| tui |
T047 |
|
| subClassOf |