Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4607740010 | Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4607741014 | Zhu Tokita Takenouchi Kim syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4607742019 | ZTTK syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4607743012 | Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4607744018 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, intellectual disability and mild to moderate facial dysmorphism in association with variable brain malformations including abnormal gyration patterns, ventriculomegaly, white matter abnormalities, hypoplasia of the corpus callosum and cerebellar hemispheres. Musculoskeletal abnormalities include hemivertebrae, scoliosis or kyphosis, contractures, and joint laxity. Ocular involvement includes strabismus, hypermetropia and cortical visual impairment. Hypotonia may also be associated. Additional clinical manifestations may include seizures, short stature urogenital malformations, heart defects and gastrointestinal malformations. The disorder is due to a heterozygous de novo SON mutation (21q22.11), which encodes for a protein required for proper RNA splicing. Whilst the disease is autosomal dominant, all reported cases have occurred sporadically. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Interprets | Intellectual ability | true | Inferred relationship | Some | 2 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Interprets | Adaptation behaviour | true | Inferred relationship | Some | 3 | |
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set