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771184001: Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3704804017 Leukoencephalopathy, palmoplantar keratoderma syndrome en Synonym Active Case insensitive SNOMED CT core
3704805016 Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3789564010 Leucoencephalopathy, palmoplantar keratoderma syndrome en Synonym Active Case insensitive SNOMED CT core
3704806015 A rare genetic epidermal disease with characteristics of early childhood-onset of punctate palmoplantar keratoderma in association with adult-onset leukoencephalopathy manifested by progressive tetrapyramidal syndrome and cognitive deterioration. en Definition Active Case sensitive SNOMED CT core
3789563016 A rare genetic epidermal disease with characteristics of early childhood-onset of punctate palmoplantar keratoderma in association with adult-onset leucoencephalopathy manifested by progressive tetrapyramidal syndrome and cognitive deterioration. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 4
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure of palmar area of hand true Inferred relationship Some 4
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Inherited disorder of keratinisation true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure of sole of foot true Inferred relationship Some 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Keratosis false Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Rough skin false Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Rough skin of hands true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Leukoencephalopathy true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Punctate palmoplantar keratoderma true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Interprets Keratinisation true Inferred relationship Some 1
Leukoencephalopathy, palmoplantar keratoderma syndrome Has interpretation Abnormal true Inferred relationship Some 1
Leukoencephalopathy, palmoplantar keratoderma syndrome Is a Hereditary disorder of the integument false Inferred relationship Some
Leukoencephalopathy, palmoplantar keratoderma syndrome Occurrence Adulthood false Inferred relationship Some 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Cerebral white matter structure true Inferred relationship Some 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Occurrence Early childhood false Inferred relationship Some 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Finding site Skin structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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