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402851000: Neonatal purpura fulminans due to homozygous protein C deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1770775011 Neonatal purpura fulminans (homozygous protein C deficiency) (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
1781943015 Neonatal purpura fulminans (homozygous protein C deficiency) en Synonym Inactive Only initial character case insensitive SNOMED CT core module
5136952018 Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5136953011 Neonatal purpura fulminans due to homozygous protein C deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal purpura fulminans due to homozygous protein C deficiency Is a Purpura fulminans true Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Blood vessel structure of skin false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Course Acute fulminating false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Purpura false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier 1
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Structure of skin region false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Necrosis false Inferred relationship Existential restriction modifier 2
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Thrombus false Inferred relationship Existential restriction modifier 1
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Neonatal purpura fulminans due to homozygous protein C deficiency Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Clinical course Acute fulminating true Inferred relationship Existential restriction modifier 4
Neonatal purpura fulminans due to homozygous protein C deficiency Has definitional manifestation Purpura false Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Thrombus true Inferred relationship Existential restriction modifier 1
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Necrosis true Inferred relationship Existential restriction modifier 2
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Structure of capillary blood vessel true Inferred relationship Existential restriction modifier 1
Neonatal purpura fulminans due to homozygous protein C deficiency Is a Homozygous protein C deficiency true Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Associated morphology Purpura true Inferred relationship Existential restriction modifier 3
Neonatal purpura fulminans due to homozygous protein C deficiency Finding site Skin structure true Inferred relationship Existential restriction modifier 3
Neonatal purpura fulminans due to homozygous protein C deficiency Interprets Hemostatic function true Inferred relationship Existential restriction modifier 5
Neonatal purpura fulminans due to homozygous protein C deficiency Has interpretation Abnormal true Inferred relationship Existential restriction modifier 5
Neonatal purpura fulminans due to homozygous protein C deficiency Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Neonatal purpura fulminans due to homozygous protein C deficiency Due to Homozygous protein C deficiency true Inferred relationship Existential restriction modifier 6
Neonatal purpura fulminans due to homozygous protein C deficiency Is a Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder 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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