Descriptions:
Term | description type | Language/acceptability | Language/acceptability | Case significance |
---|---|---|---|---|
[course] congenital [morphology] of [body structure] caused by [agent] (disorder) | FSN | us:P | gb:P | ci |
[course] Congenital [morphology] of [body structure] caused by [agent] | 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 | 246075003 |Causative agent (attribute)| | [Substance] < 105590001 |Substance (substance)| OR [Organism] < 410607006 |Organism (organism)| | 1 |
Definition status:
Applies to:
<< 276654001 |Congenital malformation (disorder)|