Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3332212014 | Intellectual disability, developmental delay, contracture syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332213016 | Intellectual disability, developmental delay, contracture syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332214010 | Foot contracture, muscle atrophy, oculomotor apraxia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332215011 | Wieacker Wolff syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3332216012 | A severe X-linked recessive neurodevelopmental disorder with the association of arthrogryposis multiplex congenita and intellectual disability. The syndrome has been reported in 5 families to date, with fewer than 30 affected individuals described. Affected patients are male, while carrier females are often asymptomatic. Facial weakness (ptosis) and bulbar weakness (feeding difficulty), characteristic dysmorphic facial and skeletal abnormalities have been reported. Other neurological signs may include spasticity and seizures. Heterozygous female carriers may also be affected, but to a lesser degree (intellectual disability, distal muscle weakness, camptodactyly, joint contractures, and pes equinovarus). Caused by mutations in the ZC4H2 gene (Xq11.1) that is presumed to play a role in neuronal function during fetal growth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 7608841000172111 | syndrome de contractures du pied, atrophie musculaire et apraxie oculomotrice | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7608851000172113 | syndrome de déficience intellectuelle, retard de développement et contractures | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7608861000172110 | syndrome de Wieacker-Wolff | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5474511000172111 | syndroom van verstandelijke beperking, ontwikkelingsachterstand en contracturen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5474521000172118 | syndroom van verstandelijke handicap, ontwikkelingsachterstand en contracturen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5474531000172115 | syndroom van mentale retardatie, ontwikkelingsachterstand en contracturen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5474541000172110 | syndroom van Wieacker-Wolff | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Inherited arthrogryposis | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | amyoplasie congénitale de Sheldon | false | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Muscle atrophy | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | retard mental | false | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 4 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 3 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Skeletal muscle structure (body structure) | false | Inferred relationship | Some | 3 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Associated morphology | Contracture | false | Inferred relationship | Some | 4 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 5 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 5 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Congenital anomaly of skeletal muscle | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Skeletal muscle structure (body structure) | true | Inferred relationship | Some | 1 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 2 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 2 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 3 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 3 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 2 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 4 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | Arthrogryposis multiplex congenita | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR