Jump to:
loading...| Preferred Name |
Blount disease |
|
| Synonyms |
Osteochondrosis deformans tibiae, familial infantile type Tibia vara Osteochondrosis Deformans Tibiae |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C536237 |
|
| altLabel |
Osteochondrosis deformans tibiae, familial infantile type Tibia vara Osteochondrosis Deformans Tibiae |
|
| cui |
C0175756 C0220757 |
|
| Has mapping qualifier | ||
| HM |
D001848 D055034/Q000151 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20100825 |
|
| MeSH Frequency |
134 |
|
| MMR |
20150817 |
|
| notation |
C536237 |
|
| prefLabel |
Blount disease |
|
| SC |
3 |
|
| Scope Statement |
A developmental condition characterized by disordered endochondral ossification of the medial part of the proximal tibial physis resulting in multiplanar deformities of the lower limb. It is a genetically heterogeneous disorder with distinct infantile (OMIM: 188700) and adolescent (OMIM: 259200) forms. |
|
| TERMUI |
T738699 T738700 T800645 T738701 |
|
| TH |
OMIM (2013) ORD (2010) |
|
| tui |
T047 |
Create mapping