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1222646006: Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5048286011 Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5048287019 Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
5048291012 Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Is a Hereditary palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Is a Hereditary motor and sensory neuropathy true Inferred relationship Existential restriction modifier
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 3
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Finding site Skin structure of sole of foot true Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Finding site Skin structure of palmar area of hand true Inferred relationship Existential restriction modifier 2
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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