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55056006: Hepatic porphyria (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
91537011 Hepatic porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
793355018 Hepatic porphyria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hepatic porphyria Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Disorder of liver true Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Porphyria false Inferred relationship Existential restriction modifier
Hepatic porphyria Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Hepatic porphyria Occurrence Congenital false Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Disorder of porphyrin metabolism false Inferred relationship Existential restriction modifier
Hepatic porphyria Is a Porphyria true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Variegate porphyria Is a True Hepatic porphyria Inferred relationship Existential restriction modifier
Porphyria cutanea tarda Is a True Hepatic porphyria Inferred relationship Existential restriction modifier
Benign recurrent intrahepatic cholestasis Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Rotor syndrome Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Dubin-Johnson syndrome Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Familial arthrogryposis-cholestatic hepatorenal syndrome Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Progressive intrahepatic cholestasis Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Crigler-Najjar syndrome, type I Is a False Hepatic porphyria Inferred relationship Existential restriction modifier
Hereditary coproporphyria Is a True Hepatic porphyria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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