Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
17743010 |
Triploidy, diploidy, mixoploidy syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
533866015 |
Triploidy, diploidy, mixoploidy syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
17743010 |
Triploidy, diploidy, mixoploidy syndrome |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
17743010 |
Triploidy, diploidy, mixoploidy syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
533866015 |
Triploidy, diploidy, mixoploidy syndrome (disorder) |
en |
Fully specified name |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
533866015 |
Triploidy, diploidy, mixoploidy syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4423011000241118 |
syndrome de triploïdie, diploïdie, mixoploïdie |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
4423011000241118 |
syndrome de triploïdie, diploïdie, mixoploïdie |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Is a |
Congenital chromosomal disease |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
Triploidy |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
Alteration of chromosome structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Finding site |
Chromosome structure (cell structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
anomalie congénitale |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
anomalie congénitale |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Finding site |
Chromosome structure (cell structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Finding site |
Chromosome structure (cell structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Triploidy, diploidy, mixoploidy syndrome (disorder) |
Associated morphology |
Triploidy |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|