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771184001: Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3704804017 Leukoencephalopathy, palmoplantar keratoderma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3704805016 Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3789564010 Leucoencephalopathy, palmoplantar keratoderma 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
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Leukoencephalopathy true Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Punctate palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, palmoplantar keratoderma syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Occurrence Adulthood false Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Cerebral white matter structure true Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Occurrence Early childhood false Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 4
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure of palmar area of hand true Inferred relationship Existential restriction modifier 4
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Inherited disorder of keratinization true Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure of sole of foot true Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Keratosis false Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Rough skin false Inferred relationship Existential restriction modifier
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Rough skin of hands true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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