Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
5183247010 |
Craniosynostosis, microretrognathia, severe intellectual disability syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5183248017 |
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5400680014 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro-/retrognathia, cleft palate, and brachydactyly, and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones, and pathological fractures), and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5400681013 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro-/retrognathia, cleft palate, and brachydactyly, and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones, and pathological fractures), and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5183247010 |
Craniosynostosis, microretrognathia, severe intellectual disability syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5183248017 |
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5183249013 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro/retrognathia, cleft palate, brachydactyly and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones and pathological fractures) and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5400680014 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro-/retrognathia, cleft palate, and brachydactyly, and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones, and pathological fractures), and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5400681013 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro-/retrognathia, cleft palate, and brachydactyly, and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones, and pathological fractures), and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Congenital retrognathism |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Autosomal dominant hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Congenital anomaly of bone and joint |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Severe mental retardation (I.Q. 20-34) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Craniosynostosis syndrome |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Is a |
Multiple malformation syndrome with facial defects as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Interprets |
Intellectual ability (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Interprets |
Adaptation behavior |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Finding site |
Joint structure of suture of skull |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Associated morphology |
Congenital premature fusion |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Finding site |
Bone structure of jaw (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Associated morphology |
Recession |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder) |
Associated morphology |
Premature fusion (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|