| Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
| 3704819016 |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 3704820010 |
Arthropathy camptodactyly syndrome |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 3704821014 |
Pericarditis, arthropathy, camptodactyly syndrome |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 3704822019 |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 3704823012 |
Jacobs syndrome |
en |
Synonym |
Active |
Entire term case sensitive |
SNOMED CT core module |
| 3704824018 |
CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome |
en |
Synonym |
Active |
Entire term case sensitive |
SNOMED CT core module |
| 3704825017 |
CACP syndrome |
en |
Synonym |
Active |
Entire term case sensitive |
SNOMED CT core module |
| Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Is a |
Flexion deformity of finger |
false |
Inferred relationship |
Existential restriction modifier |
|
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Finding site |
Proximal interphalangeal joint of finger structure |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Is a |
Polyarthropathy |
true |
Inferred relationship |
Existential restriction modifier |
|
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Associated morphology |
Flexion deformity |
false |
Inferred relationship |
Existential restriction modifier |
1 |
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier |
|
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier |
|
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Finding site |
Joint structure of multiple body sites |
true |
Inferred relationship |
Existential restriction modifier |
2 |
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Associated morphology |
Fixed flexion deformity |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome |
Is a |
Fixed flexion deformity finger |
true |
Inferred relationship |
Existential restriction modifier |
|
|