Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3498667014 |
Absent tibia, polydactyly, arachnoid cyst syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3498668016 |
Holmes Collins syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498669012 |
Absent tibia, polydactyly, arachnoid cyst syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5403709019 |
Tibia absent - polydactyly - arachnoid cyst syndrome is a very rare constellation of multiple anomalies, including absence or hypoplasia of the tibia. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498667014 |
Absent tibia, polydactyly, arachnoid cyst syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3498668016 |
Holmes Collins syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498669012 |
Absent tibia, polydactyly, arachnoid cyst syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3499956018 |
A very rare constellation of multiple anomalies including absence or hypoplasia of the tibia. It has been described in 3 siblings (two males and one female). The syndrome has characteristics of the absence or hypoplasia of the tibia, pre and postaxial polydactyly of the hands and/or feet, syndactyly of the toes, shortening and bowing of other long bones, and retrocerebellar arachnoid cyst. Parental consanguinity reported in the family suggests an autosomal recessive pattern of inheritance. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403709019 |
Tibia absent - polydactyly - arachnoid cyst syndrome is a very rare constellation of multiple anomalies, including absence or hypoplasia of the tibia. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3442981001000114 |
Tibia, fehlende - Polydaktylie - arachnoide Zysten |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
886141000172113 |
syndrome de tibia absent-polydactylie-kyste arachnoïdien |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
915141000172112 |
syndrome de Holmes-Collins |
fr |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
886141000172113 |
syndrome de tibia absent-polydactylie-kyste arachnoïdien |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
915141000172112 |
syndrome de Holmes-Collins |
fr |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3442981001000114 |
Tibia, fehlende - Polydaktylie - arachnoide Zysten |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Arachnoid cyst |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Multiple malformation syndrome with limb defect as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Congenital anomaly of tibia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Connective tissue hereditary disorder |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Hereditary disorder of nervous system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Polydactyly (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
anomalie du développement |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Bone structure of tibia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Supernumerary structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Digit structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Cyst (morphologic abnormality) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Arachnoid structure (body structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Supernumerary structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Digit structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Congenital malformation of the meninges |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Bone structure of tibia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Cyst (morphologic abnormality) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Finding site |
Arachnoid structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Associated morphology |
Arachnoid cyst (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Absent tibia, polydactyly, arachnoid cyst syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|