Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5066437013 | Frontorhiny (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5066438015 | ALX3-related frontonasal dysplasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
5066439011 | Frontorhiny | en | Synonym | Active | Case insensitive | SNOMED CT core |
5066440013 | ALX homeobox 3-related frontonasal dysplasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
5066441012 | Isolated median cleft face syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
5066442017 | Frontonasal dysplasia type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
5066443010 | A distinct syndromic type of frontonasal malformation with characteristics of hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set