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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

Scg expression
116680003\|Is a (attribute)\|

Scg expression
64572001\|Disease (disorder)\|

0

N/A

0..1

Scg expression
263502005\|Clinical course (attribute)\|

[Course] < 288524001 |Courses (qualifier value)|

0

N/A

1..1

Scg expression
246454002\|Occurrence (attribute)\|

Scg expression
255399007\|Congenital (qualifier value)\|

1

1..1

0..1

Scg expression
116676008\|Associated morphology (attribute)\|

Scg expression
<49755003\|Morphologically abnormal structure (morphologic abnormality)\|

1

0..1

Scg expression
363698007\|Finding site (attribute)\|

Scg expression
<442083009\|Anatomical or acquired body structure (body structure)\|

1

1..1

Scg expression
370135005 \|Pathological process (attribute)\|

Scg expression
<< 308490002 \|Pathological developmental process (qualifier value)\|

1

0..1

246075003 |Causative agent (attribute)|

[Substance] < 105590001 |Substance (substance)|

OR

[Organism] < 410607006 |Organism (organism)|

1

Definition status:

Scg expression
900000000000073002\|Defined\|

Applies to:

Scg expression
<< 276654001\|Congenital malformation (disorder)\|

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Descriptions:

Concept model:

Definition status:

Applies to:

Template Language:

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