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722203001: Palmoplantar keratoderma with deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3331138017 Palmoplantar keratoderma with deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331139013 Palmoplantar keratoderma with deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331140010 A keratinization disorder characterized by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenar, hypothenar and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. The disease is transmitted in an autosomal dominant manner with incomplete penetrance. Caused by heterozygous mutation in the gene encoding connexin-26 (GJB2; 121011) on chromosome 13q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331141014 A keratinisation disorder characterised by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenar, hypothenar and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. The disease is transmitted in an autosomal dominant manner with incomplete penetrance. Caused by heterozygous mutation in the gene encoding connexin-26 (GJB2; 121011) on chromosome 13q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
983241000172117 syndrome KPP(kératodermie palmoplantaire)-surdité fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
1017141000172112 syndrome de kératodermie palmoplantaire-surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
873541000172118 palmoplantaire keratodermie, doofheidsyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1016641000172118 hyperkeratose van handpalm en voetzool, doofheidsyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Sensorineural hearing loss true Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Congenital hearing disorder false Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Hereditary palmoplantar keratoderma true Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 3
Palmoplantar keratoderma with deafness syndrome (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Interprets Hearing true Inferred relationship Some 4
Palmoplantar keratoderma with deafness syndrome (disorder) Interprets Functional observable false Inferred relationship Some
Palmoplantar keratoderma with deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Some 6
Palmoplantar keratoderma with deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Some 6
Palmoplantar keratoderma with deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Some 7
Palmoplantar keratoderma with deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Some 7
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 6
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology Hyperkeratosis false Inferred relationship Some 7
Palmoplantar keratoderma with deafness syndrome (disorder) Interprets Keratinization false Inferred relationship Some 2
Palmoplantar keratoderma with deafness syndrome (disorder) Has interpretation Abnormal false Inferred relationship Some 2
Palmoplantar keratoderma with deafness syndrome (disorder) Finding site Skin structure of sole of foot (body structure) true Inferred relationship Some 2
Palmoplantar keratoderma with deafness syndrome (disorder) Finding site Skin structure of palmar area of hand true Inferred relationship Some 5
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology Hyperkeratosis true Inferred relationship Some 2
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology Hyperkeratosis true Inferred relationship Some 5
Palmoplantar keratoderma with deafness syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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