loading...| Preferred Name | Radioulnar Synostosis | |
| Synonyms |
Radio-ulnar synostosis type 2 Congenital radio-ulnar synostosis Radio-ulnar synostosis type 1 |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C562408 |
|
| altLabel |
Radio-ulnar synostosis type 2 Congenital radio-ulnar synostosis Radio-ulnar synostosis type 1 |
|
| cui |
C0158761 C2931148 C2931147 |
|
| Has mapping qualifier | ||
| HM |
D013580 D014457/Q000002 D011884/Q000002 |
|
| Inverse of RB |
0 |
|
| Mapped to |
http://purl.bioontology.org/ontology/MESH/D013580 |
|
| MDA |
20121105 |
|
| MeSH Frequency |
78 |
|
| MMR |
20230801 |
|
| notation |
C562408 |
|
| prefLabel |
Radioulnar Synostosis |
|
| SC |
3 |
|
| Scope Statement |
Synostosis affecting the RADIUS and ULNA characterized by limited forearm pronation and supination; limited elbow extension in Type 2. Radiologic examination shows proximal, smooth radioulnar fusion with absent radial head in Type 1 or radioulnar fusion distal to the proximal radial epiphysis with congenital radial head dislocation (Type 2). Inheritance may be autosomal dominant. it also is a feature of certain chromosome abnormalities, such as triple X-Y syndrome (XXXY). OMIM: 179300 |
|
| TERMUI |
T738788 T800635 T738790 T738787 |
|
| TH |
OMIM (2013) ORD (2010) |
|
| tui |
T047 T019 |