Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3756672013 |
Brachydactyly, short stature, retinitis pigmentosa syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3756673015 |
Brachydactyly, short stature, retinitis pigmentosa syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3756674014 |
A rare genetic congenital limb malformation syndrome with characteristics of mild to severe short stature, brachydactyly and retinal degeneration (usually retinitis pigmentosa) associated with variable intellectual disability, developmental delay and craniofacial anomalies. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the CWC27 gene on chromosome 5q12. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3756672013 |
Brachydactyly, short stature, retinitis pigmentosa syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3756673015 |
Brachydactyly, short stature, retinitis pigmentosa syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3756674014 |
A rare genetic congenital limb malformation syndrome with characteristics of mild to severe short stature, brachydactyly and retinal degeneration (usually retinitis pigmentosa) associated with variable intellectual disability, developmental delay and craniofacial anomalies. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the CWC27 gene on chromosome 5q12. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3417681001000111 |
Brachydaktylie-Kleinwuchs-Retinitis pigmentosa-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
5806991000241110 |
syndrome de brachydactylie, petite taille et rétinite pigmentaire |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
5806991000241110 |
syndrome de brachydactylie, petite taille et rétinite pigmentaire |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3417681001000111 |
Brachydaktylie-Kleinwuchs-Retinitis pigmentosa-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 |
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Hereditary disorder of the visual system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Degeneration of retina (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Finding site |
Bone structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Brachydactyly |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Short stature disorder (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Dysostosis |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Finding site |
Digit structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Associated morphology |
Abnormally short growth |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Associated morphology |
dégénérescence |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Finding site |
Retinal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Associated morphology |
Degenerative abnormality (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Brachydactyly, short stature, retinitis pigmentosa syndrome |
Interprets |
Height / growth measure (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|