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59229005: Familial porphyria cutanea tarda (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
98397018 Familial porphyria cutanea tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
98398011 Hereditary porphyria cutanea tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
798048011 Familial porphyria cutanea tarda (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5247305010 PCT (porphyria cutanea tarda) type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


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 Some
Familial porphyria cutanea tarda Occurrence Congenital false Inferred relationship Some
Familial porphyria cutanea tarda Finding site Skin structure true Inferred relationship Some 2
Familial porphyria cutanea tarda Finding site Liver structure true Inferred relationship Some 1
Familial porphyria cutanea tarda Is a Familial disease true Inferred relationship Some
Familial porphyria cutanea tarda Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial porphyria cutanea tarda Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Familial porphyria cutanea tarda Is a Hereditary disorder of the integument true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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