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785725008: Palmoplantar keratoderma, spastic paralysis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3768166017 Palmoplantar keratoderma, spastic paralysis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768167014 Palmoplantar keratoderma, spastic paralysis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768168016 Powell Venencie Gordon syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3768169012 A rare genetic punctate palmoplantar keratoderma disease with characteristics of discrete focal punctate keratoderma on the palms and soles and/or slowly progressive spastic paralysis, predominantly affecting the lower limbs. Lesional histology reveals pronounced orthokeratosis, acanthosis, papillomatosis, and regular undulation to the surface keratin. There have been no further descriptions in the literature since 1983. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3768166017 Palmoplantar keratoderma, spastic paralysis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768167014 Palmoplantar keratoderma, spastic paralysis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768168016 Powell Venencie Gordon syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3768169012 A rare genetic punctate palmoplantar keratoderma disease with characteristics of discrete focal punctate keratoderma on the palms and soles and/or slowly progressive spastic paralysis, predominantly affecting the lower limbs. Lesional histology reveals pronounced orthokeratosis, acanthosis, papillomatosis, and regular undulation to the surface keratin. There have been no further descriptions in the literature since 1983. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3391851001000117 Palmoplantarkeratose-spastische Paralyse-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436411000241111 syndrome d'hyperkératose palmoplantaire et paralysie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436421000241116 syndrome de kératodermie palmoplantaire et paralysie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436431000241119 syndrome de Powell-Venencie-Gordon fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436411000241111 syndrome d'hyperkératose palmoplantaire et paralysie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436421000241116 syndrome de kératodermie palmoplantaire et paralysie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6436431000241119 syndrome de Powell-Venencie-Gordon fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391851001000117 Palmoplantarkeratose-spastische Paralyse-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Palmoplantar keratoderma, spastic paralysis syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Palmoplantar keratoderma, spastic paralysis syndrome Interprets Keratinisation true Inferred relationship Existential restriction modifier (core metadata concept) 2
Palmoplantar keratoderma, spastic paralysis syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma, spastic paralysis syndrome Is a Punctate palmoplantar keratoderma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Palmoplantar keratoderma, spastic paralysis syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Palmoplantar keratoderma, spastic paralysis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma, spastic paralysis syndrome Is a Inherited disorder of keratinisation true Inferred relationship Existential restriction modifier (core metadata concept)
Palmoplantar keratoderma, spastic paralysis syndrome Finding site Skin structure of sole of foot (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma, spastic paralysis syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Palmoplantar keratoderma, spastic paralysis syndrome Is a Keratosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Palmoplantar keratoderma, spastic paralysis syndrome Finding site Skin structure of palmar area of hand true Inferred relationship Existential restriction modifier (core metadata concept) 3
Palmoplantar keratoderma, spastic paralysis syndrome Is a Rough skin (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Palmoplantar keratoderma, spastic paralysis syndrome Is a Rough skin of hands (finding) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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