Descriptions:
| Term | description type | Language/acceptability | Language/acceptability | Case significance |
|---|---|---|---|---|
| Congenital [morphology] of [body structure] (disorder) | FSN | us:P | gb:P | ci |
| Congenital [morphology] of [body structure] | SYN | us:P | gb:P | ci |
Concept model:
| Attribute cardinality | Attribute | Value | Role group number | Role group cardinality |
|---|---|---|---|---|
| 1..1 | 0 | N/A | ||
| 0..1 | [Course] < 288524001 |Courses (qualifier value)| | 0 | N/A | |
| 1..1 | 1 | 1..1 | ||
| 0..1 | 1 | |||
| 0..1 | 1 | |||
| 1..1 | 1 | |||
| 0..1 | [Substance] < 105590001 |Substance (substance)| OR [Organism] < 410607006 |Organism (organism)| | 1 |
Definition status:
900000000000073002 |Defined (core metadata concept)|
Applies to:
<
66091009 |Congenital disease (disorder)|
Rules for description generation:
- Remove the semantic tag, e.g. (disorder)
- Remove 'congenital' from value of associated morphology.