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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 (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

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

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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