Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4669003011 | Complex neurodevelopmental disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4669004017 | Non-specific syndromic intellectual disability | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4669005016 | Non-specific syndromic intellectual disability (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4669006015 | A rare genetic intellectual disability characterised by the association of intellectual disability with variable other anomalies in the absence of a well-characterised syndrome. Associated abnormalities may include facial dysmorphism, neurological signs and symptoms, behavioural problems, and abnormalities of various other organ systems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4669007012 | A rare genetic intellectual disability characterized by the association of intellectual disability with variable other anomalies in the absence of a well-characterized syndrome. Associated abnormalities may include facial dysmorphism, neurological signs and symptoms, behavioral problems, and abnormalities of various other organ systems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Non-specific syndromic intellectual disability | est un(e) (attribut) | Intellectual disability | true | Inferred relationship | Some | ||
| Non-specific syndromic intellectual disability | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Non-specific syndromic intellectual disability | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Juberg Marsidi syndrome (disorder) | est un(e) (attribut) | True | Non-specific syndromic intellectual disability | Inferred relationship | Some |
This concept is not in any reference sets
FHIR