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402851000: neonatale purpura fulminans bij homozygote proteïne C-deficiëntie (aandoening)

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
8636691000146112 neonatale purpura fulminans bij homozygote proteïne C-deficiëntie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8723221000146110 neonatale purpura fulminans bij homozygote proteïne C-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10027541000146113 purpura fulminans bij pasgeborene door homozygote deficiëntie van proteïne C nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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 Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Blood vessel structure of skin (body structure) false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Course Acute fulminating false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Purpura false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Some 1
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Structure of skin region false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Necrosis false Inferred relationship Some 2
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Thrombus (morphologic abnormality) false Inferred relationship Some 1
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Skin structure false Inferred relationship Some 2
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Has definitional manifestation Hemostatic system finding false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Clinical course Acute fulminating true Inferred relationship Some 4
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Has definitional manifestation purpura false Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Thrombus (morphologic abnormality) true Inferred relationship Some 1
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Skin structure true Inferred relationship Some 2
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Necrosis true Inferred relationship Some 2
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Structure of capillary blood vessel true Inferred relationship Some 1
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Is a Homozygous protein C deficiency (disorder) true Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Associated morphology Purpura true Inferred relationship Some 3
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site Skin structure true Inferred relationship Some 3
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Interprets Hemostatic function true Inferred relationship Some 5
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Has interpretation Abnormal true Inferred relationship Some 5
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Due to Homozygous protein C deficiency (disorder) true Inferred relationship Some 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 Some
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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