Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3662960019 | Finucane Kurtz Scott syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3662961015 | Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3662962010 | Epiphyseal dysplasia, hearing loss, dysmorphism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3664260010 | A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Severe behaviour disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns are also associated. There have been no further descriptions in the literature since 1992. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3664261014 | A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Severe behavior disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns are also associated. There have been no further descriptions in the literature since 1992. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Multiple malformation syndrome with facial-limb defects as major feature | true | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | dysgenese | false | Inferred relationship | Some | 3 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 3 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Sensorineural hearing loss | false | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Interprets | træk vedr. funktion | false | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Epiphyseal dysplasia | true | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 5 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | kongenit dysplasi | false | Inferred relationship | Some | 2 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | dysgenese | false | Inferred relationship | Some | 4 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Finding site | Structure of epiphysis | true | Inferred relationship | Some | 2 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Finding site | Ear structure | true | Inferred relationship | Some | 1 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Finding site | Limb structure | true | Inferred relationship | Some | 4 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 4 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 2 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Chronic mental disorder | false | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Chronic disease of ear | false | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Congenital sensorineural hearing loss (disorder) | true | Inferred relationship | Some | ||
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 6 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 7 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 7 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 8 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 8 | |
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) | Is a | Chronic deafness | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets