loading...| Preferred Name |
Arthrogryposis multiplex congenita |
|
| Synonyms |
Multiple congenital arthrogryposis Arthrogryposis multiplex congenita (disorder) |
|
| Definitions |
A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/205402004 |
|
| Active |
1 |
|
| altLabel |
Multiple congenital arthrogryposis AMC - arthrogryposis multiplex congenita Arthrogryposis multiplex congenita (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005 |
|
| CTV3ID |
PFy0. |
|
| cui |
C5779613 |
|
| definition |
A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20230228 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has interpretation | ||
| Has pathological process | ||
| INACTIVATION INDICATOR |
900000000000482003 900000000000495008 |
|
| interprets | ||
| notation |
205402004 |
|
| Occurs in | ||
| prefLabel |
Arthrogryposis multiplex congenita |
|
| Subset member |
900000000000497000~MAPTARGET~PFy0. 447562003~MAPRULE~TRUE 900000000000527005~TARGETCOMPONENT~77016009 900000000000490003~VALUEID~900000000000495008 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 900000000000489007~VALUEID~900000000000482003 447562003~CORRELATIONID~447561005 900000000000509007~ACCEPTABILITYID~900000000000548007 447562003~MAPADVICE~ALWAYS Q74.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 447562003~MAPTARGET~Q74.3 900000000000509007~ACCEPTABILITYID~900000000000549004 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |