Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
4697279019 |
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4697280016 |
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5399766018 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints, and pes planovalgus. Seizures and episodes of aggressive behavior during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399767010 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints, and pes planovalgus. Seizures and episodes of aggressive behaviour during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697279019 |
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4697280016 |
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4697282012 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints and pes planovalgus. Seizures and episodes of aggressive behavior during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697283019 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints and pes planovalgus. Seizures and episodes of aggressive behaviour during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399766018 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints, and pes planovalgus. Seizures and episodes of aggressive behavior during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399767010 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by profound intellectual disability, hypotonia, coarse facial features, strabismus and impaired visual fixation, hypermobility of interphalangeal joints, contractures in the elbow joints, and pes planovalgus. Seizures and episodes of aggressive behaviour during sleep have also been reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3394631001000112 |
Schwere Intelligenzminderung-Hypotonie-Strabismus-grobe Gesichtsszüge-Planovalgus-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3394631001000112 |
Schwere Intelligenzminderung-Hypotonie-Strabismus-grobe Gesichtsszüge-Planovalgus-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 |
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Congenital valgus deformity of foot |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Multiple malformation syndrome with facial-limb defects as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Hereditary disorder of the visual system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Severe mental retardation (I.Q. 20-34) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Is a |
Congenital strabismus |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Finding site |
Eye region structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Finding site |
Face structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Finding site |
Foot structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Associated morphology |
Planovalgus |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Interprets |
Intellectual ability (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Interprets |
Adaptation behavior |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|