Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3723483016 | Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3723484010 | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3723485011 | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3723486012 | A rare genetic syndromic intellectual disability disorder characterized by severe intellectual disability with limited or absent speech and language, short stature, acquired microcephaly, kyphoscoliosis or scoliosis, and behavioral disturbances that include hyperactivity, stereotypy and aggressiveness. Facial dysmorphism typically includes sloping forehead, mild synophrys, deep-set eyes, strabismus, anteverted large ears, prominent nose and dental malposition. Caused by homozygous mutation in the TTI2 gene on chromosome 8p12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3723487015 | A rare genetic syndromic intellectual disability disorder characterised by severe intellectual disability with limited or absent speech and language, short stature, acquired microcephaly, kyphoscoliosis or scoliosis, and behavioural disturbances that include hyperactivity, stereotypy and aggressiveness. Facial dysmorphism typically includes sloping forehead, mild synophrys, deep-set eyes, strabismus, anteverted large ears, prominent nose and dental malposition. Caused by homozygous mutation in the TTI2 gene on chromosome 8p12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Is a | Short stature disorder | true | Inferred relationship | Some | ||
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Interprets | Height / growth measure | true | Inferred relationship | Some | 2 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets