Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3442892016 | Autosomal recessive faciodigitogenital syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3442893014 | Autosomal recessive facio-digito-genital syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3442894015 | Aarskog-like syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3442895019 | Autosomal recessive faciodigitogenital syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3442896018 | Facio-digito-genital syndrome Kuwait type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3442897010 | Teebi Naguib Alawadi syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3442898017 | A very rare syndrome including short stature, facial dysmorphism, hand abnormalities and shawl scrotum. It has been observed in 16 subjects from five distantly related sibships of a large Kuwaiti Bedouin tribe. The affected patients had no intellectual deficit. Transmitted as an autosomal recessive trait. | 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