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722203001: syndrome de kératodermie palmoplantaire-surdité (trouble)


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
1017141000172112 syndrome de kératodermie palmoplantaire-surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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
758341000241114 syndrome de kératodermie palmoplantaire-surdité (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
983241000172117 syndrome KPP(kératodermie palmoplantaire)-surdité fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
syndrome de kératodermie palmoplantaire-surdité localisation d'une constatation (attribut) Skin structure of sole of foot true Inferred relationship Some 2
syndrome de kératodermie palmoplantaire-surdité localisation d'une constatation (attribut) peau de la région palmaire de la main (structure corporelle) true Inferred relationship Some 5
syndrome de kératodermie palmoplantaire-surdité morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 2
syndrome de kératodermie palmoplantaire-surdité morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 5
syndrome de kératodermie palmoplantaire-surdité a pour interprétation (attribut) altéré true Inferred relationship Some 4
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Sensorineural hearing loss true Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Congenital hearing disorder false Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Hereditary palmoplantar keratoderma true Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Auditory system hereditary disorder true Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité localisation d'une constatation (attribut) structure du système auditif true Inferred relationship Some 3
syndrome de kératodermie palmoplantaire-surdité est défini par la manifestation de (attribut) Abnormal keratinisation false Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité interprète (attribut) Hearing, function (observable entity) true Inferred relationship Some 4
syndrome de kératodermie palmoplantaire-surdité interprète (attribut) entité observable fonctionnelle false Inferred relationship Some
syndrome de kératodermie palmoplantaire-surdité survenue (attribut) congénital false Inferred relationship Some 6
syndrome de kératodermie palmoplantaire-surdité localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 6
syndrome de kératodermie palmoplantaire-surdité survenue (attribut) congénital false Inferred relationship Some 7
syndrome de kératodermie palmoplantaire-surdité localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 7
syndrome de kératodermie palmoplantaire-surdité morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 6
syndrome de kératodermie palmoplantaire-surdité morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 7
syndrome de kératodermie palmoplantaire-surdité interprète (attribut) Keratinization, function (observable entity) false Inferred relationship Some 2
syndrome de kératodermie palmoplantaire-surdité a pour interprétation (attribut) anormal false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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