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59229005: Familial porphyria cutanea tarda (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
98397018 Familial porphyria cutanea tarda en Synonym Active Entire term case insensitive SNOMED CT core module
98398011 Hereditary porphyria cutanea tarda en Synonym Active Entire term case insensitive SNOMED CT core module
98399015 PCT, type II en Synonym Active Entire term case sensitive SNOMED CT core module
798048011 Familial porphyria cutanea tarda (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial porphyria cutanea tarda Is a Porphyria cutanea tarda true Inferred relationship Existential restriction modifier
Familial porphyria cutanea tarda Occurrence Congenital false Inferred relationship Existential restriction modifier
Familial porphyria cutanea tarda Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Familial porphyria cutanea tarda Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Familial porphyria cutanea tarda Is a Familial disease true Inferred relationship Existential restriction modifier
Familial porphyria cutanea tarda Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial porphyria cutanea tarda Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Familial porphyria cutanea tarda Is a Hereditary disorder of the integument 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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