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717183001: Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308613015 Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308614014 Keratoderma hereditarium mutilans with ichthyosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308615010 Camisa disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308616011 Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308617019 Vohwinkel ichthyosis syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308618012 A diffuse palmoplantar keratoderma with manifestation of honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness.Follows an autosomal dominant mode of transmission. 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
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 1
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) Autosomal dominant ichthyosis (disorder) true Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) Erythrokeratodermia variabilis false Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) Entire skin true Inferred relationship Some 1
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) peau de la région palmaire de la main (structure corporelle) false Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) interprète (attribut) Keratinization, function (observable entity) false Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) Skin structure of sole of foot false Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) interprète (attribut) Keratinization, function (observable entity) false Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 5
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) peau de la région palmaire de la main (structure corporelle) true Inferred relationship Some 5
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 6
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) Skin structure of sole of foot true Inferred relationship Some 6
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) Mutilating keratoderma true Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) interprète (attribut) Hearing, function (observable entity) true Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) a pour interprétation (attribut) altéré true Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) structure du système auditif true Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) Congenital keratoderma true Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) ichtyose congénitale false Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) Autosomal dominant mutilating keratoderma false Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est défini par la manifestation de (attribut) Abnormal keratinisation false Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 2
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) interprète (attribut) Keratinization, function (observable entity) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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