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234422006: Acute intermittent porphyria (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
351223014 Acute intermittent porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
351224015 AIP - Acute intermittent porphyria en Synonym Active Entire term case sensitive SNOMED CT core module
351225019 Pyrroloporphyria en Synonym Active Entire term case insensitive SNOMED CT core module
351226018 Acute porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
351227010 Intermittent acute porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
351228017 Swedish porphyria en Synonym Active Entire term case sensitive SNOMED CT core module
351229013 Intermittent acute porphyria syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
622738015 Acute intermittent porphyria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute intermittent porphyria Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Acute intermittent porphyria Is a Porphobilinogen deaminase deficiency true Inferred relationship Existential restriction modifier
Acute intermittent porphyria Finding site Body system structure false Inferred relationship Existential restriction modifier
Acute intermittent porphyria Occurrence Congenital false Inferred relationship Existential restriction modifier
Acute intermittent porphyria Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier
Acute intermittent porphyria Course Intermittent false Inferred relationship Existential restriction modifier
Acute intermittent porphyria Is a Porphyria true Inferred relationship Existential restriction modifier
Acute intermittent porphyria Clinical course Intermittent true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous acute intermittent porphyria Is a True Acute intermittent porphyria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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