Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
358254015 | Keratitis ichthyosis and deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
358255019 | KIDS - Keratitis ichthyosis and deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
628024010 | Keratitis ichthyosis and deafness syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1223177018 | Keratitis ichthyosis deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5144589011 | KID syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5144590019 | Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5144593017 | Ichthyosis hystrix Rheydt type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5144594011 | KID/HID syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5144591015 | A rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. Patients usually present at birth with generalized erythema and ichthyosiform scaling. The skin manifestations are progressive with erythrokeratoderma characterized by well-demarcated erythematous and keratotic plaques with a verrucous appearance predominantly located on the face, scalp, ears, elbows and knees. Hearing loss is congenital, usually sensorineural and is often profound. Caused by mutations involving the N-terminus and first extracellular loop of the GJB2 gene (13q11-q12), encoding connexin-26. Most of the reported cases are sporadic, but familial cases with autosomal dominant inheritance have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5144592010 | A rare congenital ectodermal disorder characterised by vascularising keratitis, hyperkeratotic skin lesions and hearing loss. Patients usually present at birth with generalised erythema and ichthyosiform scaling. The skin manifestations are progressive with erythrokeratoderma characterised by well-demarcated erythematous and keratotic plaques with a verrucous appearance predominantly located on the face, scalp, ears, elbows and knees. Hearing loss is congenital, usually sensorineural and is often profound. Caused by mutations involving the N-terminus and first extracellular loop of the GJB2 gene (13q11-q12), encoding connexin-26. Most of the reported cases are sporadic, but familial cases with autosomal dominant inheritance have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Cutaneous syndrome with ichthyosis | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Structure of skin region | false | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 2 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Entire skin | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Congenital hearing disorder | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Ectodermal dysplasia | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Structure of auditory system (body structure) | false | Inferred relationship | Some | 4 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 4 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 5 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 5 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Ectoderm structure | true | Inferred relationship | Some | 5 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Interprets | Hearing | false | Inferred relationship | Some | 1 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 3 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 3 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Decreased hearing (finding) | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Keratitis ichthyosis and deafness syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 4 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 4 | |
Keratitis ichthyosis and deafness syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Senter syndrome | Is a | True | Keratitis ichthyosis and deafness syndrome (disorder) | Inferred relationship | Some | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | Is a | True | Keratitis ichthyosis and deafness syndrome (disorder) | Inferred relationship | Some |
Reference Sets