Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3759768017 |
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3759769013 |
Syndactyly, polydactyly, ear lobe syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3759767010 |
A rare genetic congenital limb malformation syndrome with characteristics of complete cutaneous syndactyly between toes 1-2, ulnar polydactyly (ranging from nubbins to an almost complete additional finger) and earlobe malformations. Additionally, abnormalities along the medial border of the foot are observed on X-ray imaging. There have been no further descriptions in the literature since 1976. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3759768017 |
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3759769013 |
Syndactyly, polydactyly, ear lobe syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3759767010 |
A rare genetic congenital limb malformation syndrome with characteristics of complete cutaneous syndactyly between toes 1-2, ulnar polydactyly (ranging from nubbins to an almost complete additional finger) and earlobe malformations. Additionally, abnormalities along the medial border of the foot are observed on X-ray imaging. There have been no further descriptions in the literature since 1976. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3389131001000117 |
Syndaktylie-Polydaktylie-Ohrmuschel-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3389131001000117 |
Syndaktylie-Polydaktylie-Ohrmuschel-Syndrom |
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 |
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Polysyndactyly (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Polydactyly of fingers |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Finding site |
Toe structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Congenital abnormality of external ear |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Disorder of pinna |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Genetic disease |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Associated morphology |
Congenital abnormal fusion |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Dysostosis |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Syndactyly of toes |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Multiple malformation syndrome with limb defect as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Associated morphology |
Supernumerary structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Finding site |
Ear lobule structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Finding site |
Finger structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Finding site |
Bone structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
Congenital anomaly of lobe of ear (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Associated morphology |
Abnormally fused structure (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|