Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643606013 | Intellectual disability Wolff type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3643607016 | Intellectual disability Wolff type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3643608014 | Wolff Zimmermann syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3643610011 | A rare intellectual disability syndrome with manifestations of severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set