Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3760123011 | Conductive hearing loss, malformation of external ear syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3760124017 | Conductive deafness, malformed external ear syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3760125016 | Mengel Konigsmark syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3760128019 | Conductive hearing loss, malformation of external ear syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3760129010 | A very rare syndromic genetic deafness with characteristics of mild to moderate conductive hearing loss, dysmorphic pinnae and lip pits or dimples. The pinnae are usually small, cup-shaped with helix folded forward, and hearing loss is associated with malformed ossicles and displacement of the external auditory canal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
10604071000172114 | syndrome de perte auditive de transmission et anomalie congenitale de l'oreille externe | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
10604081000172112 | syndrome de Mengel-Konigsmark | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
10604091000172110 | syndrome de perte d'audition de conduction et malformation de l'oreille externe | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4203001000172116 | syndroom van geleidingsgehoorverlies en afwijking van uitwendig oor | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4203011000172118 | syndroom van geleidingsgehoorverlies en malformatie van auris externa | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4203021000172111 | syndroom van conductief gehoorverlies en afwijking van uitwendig oor | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4203031000172114 | syndroom van Mengel-Konigsmark | 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 |
Conductive deafness, malformed external ear syndrome | Is a | Congenital conductive hearing loss | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Interprets | Hearing | true | Inferred relationship | Some | 2 | |
Conductive deafness, malformed external ear syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Finding site | External ear structure | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Is a | Congenital abnormality of external ear | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
Conductive deafness, malformed external ear syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set