Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3702803010 | Developmental delay with autism spectrum disorder and gait instability (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3702804016 | Developmental delay with autism spectrum disorder and gait instability | en | Synonym | Active | Case insensitive | SNOMED CT core |
3702805015 | A rare genetic neurological disorder characterised by infant hypotonia and feeding difficulties, global development delay, mild to moderate intellectual disability, delayed independent ambulation, broad-based gait with arms upheld and flexed at the elbow with brisk walking or running, and limited language skills. Behaviour patterns are highly variable and range from sociable and affectionate to autistic behaviour. Caused by homozygous mutation in the HERC2 gene on chromosome 15q13. | en | Definition | Active | Case sensitive | SNOMED CT core |
3702806019 | A rare genetic neurological disorder characterized by infant hypotonia and feeding difficulties, global development delay, mild to moderate intellectual disability, delayed independent ambulation, broad-based gait with arms upheld and flexed at the elbow with brisk walking or running, and limited language skills. Behavior patterns are highly variable and range from sociable and affectionate to autistic behavior. Caused by homozygous mutation in the HERC2 gene on chromosome 15q13. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Developmental delay with autism spectrum disorder and gait instability | Pathological process | Pathological developmental process | false | Inferred relationship | Some | 2 | |
Developmental delay with autism spectrum disorder and gait instability | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Developmental delay with autism spectrum disorder and gait instability | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Developmental delay with autism spectrum disorder and gait instability | Interprets | Intellectual ability | true | Inferred relationship | Some | 2 | |
Developmental delay with autism spectrum disorder and gait instability | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Developmental delay with autism spectrum disorder and gait instability | Interprets | Adaptation behaviour | true | Inferred relationship | Some | 3 | |
Developmental delay with autism spectrum disorder and gait instability | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Developmental delay with autism spectrum disorder and gait instability | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Developmental delay with autism spectrum disorder and gait instability | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Developmental delay with autism spectrum disorder and gait instability | Is a | Global developmental delay | true | Inferred relationship | Some | ||
Developmental delay with autism spectrum disorder and gait instability | Is a | Autistic disorder of childhood onset | true | Inferred relationship | Some | ||
Developmental delay with autism spectrum disorder and gait instability | Occurrence | Childhood | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Queensland allied health indicator for intervention reference set
Clinical finding foundation reference set
Mental health disorder reference set
Problem/Diagnosis reference set