Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3728147016 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3728148014 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3728149018 |
A rare genetic neural tube defect malformation syndrome with characteristics of sacral agenesis and abnormal vertebral body ossification with normal vertebral arches associated with notochord canal persistence on ultrasonography. Additional findings include bilateral clubfoot, oligohydramnios, and single umbilical artery and in some cases increased nuchal translucency. There is evidence the disease can be caused by homozygous mutation in the T gene on chromosome 6q27. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3728147016 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3728148014 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3728149018 |
A rare genetic neural tube defect malformation syndrome with characteristics of sacral agenesis and abnormal vertebral body ossification with normal vertebral arches associated with notochord canal persistence on ultrasonography. Additional findings include bilateral clubfoot, oligohydramnios, and single umbilical artery and in some cases increased nuchal translucency. There is evidence the disease can be caused by homozygous mutation in the T gene on chromosome 6q27. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3430041001000116 |
Sakrale Agenesie-abnormale Verknöcherung der Wirbelkörper-persistierender notochordaler Kanal-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
869861000172110 |
syndrome d'agénésie sacrée-ossification anormale des corps vertébraux-persistance de la notochorde |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
869861000172110 |
syndrome d'agénésie sacrée-ossification anormale des corps vertébraux-persistance de la notochorde |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3430041001000116 |
Sakrale Agenesie-abnormale Verknöcherung der Wirbelkörper-persistierender notochordaler Kanal-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 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Hereditary disorder of nervous system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Spinal cord structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Lumbosacral region of spine structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Sacral agenesis |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Neural tube structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Hereditary disorder of musculoskeletal system |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Neural tube defect |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Multiple system malformation syndrome |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Associated morphology |
Agenesis (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Entire sacral vertebral column |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Structure of sacral vertebral column region (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Is a |
Congenital anomaly of spinal cord |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) |
Finding site |
Entire sacral vertebral column region |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|