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59229005: Familial porphyria cutanea tarda (disorder)


Status: current. Date: 31-Jan 2002

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
98399015 PCT, type II en Synonym (core metadata concept) Inactive Entire term case sensitive (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 Autosomal dominant hereditary disorder true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Familial porphyria cutanea tarda Is a Familial disease true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Familial porphyria cutanea tarda Is a Porphyria cutanea tarda true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Familial porphyria cutanea tarda Finding site Liver structure true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly 1
Familial porphyria cutanea tarda Finding site Skin structure true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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