Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT code

SNOMED code

402851000

name

Neonatal purpura fulminans due to homozygous protein C deficiency

status

active

date introduced

2003-07-31

fully specified name(s)

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

synonyms

Neonatal purpura fulminans due to homozygous protein C deficiency

attributes - group5

Interprets

Hemostatic function 74848003

Has interpretation

Abnormal 263654008

attributes - group6

Due to

Homozygous protein C deficiency 441188004

attributes - group4

Clinical course

Acute fulminating 18131002

attributes - group1

Associated morphology

Thrombus 396339007

Finding site

Structure of capillary blood vessel 20982000

attributes - group2

Finding site

Skin structure 39937001

Associated morphology

Necrosis 6574001

attributes - group3

Associated morphology

Purpura 12393003

Finding site

Skin structure 39937001

parents

Purpura fulminans 13507004
Cardiovascular system hereditary disorder 363005004
Hereditary disorder of the integument 363185004
Homozygous protein C deficiency 441188004
Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder 724854007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Acute disease 2704003
Acute skin disorder 127334004
Purpura fulminans 13507004
Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT Concept 138875005
Clinical finding 404684003
Cardiovascular finding 106063007
Disorder of cardiovascular system 49601007
Cardiovascular system hereditary disorder 363005004
Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT Concept 138875005
Clinical finding 404684003
Functional finding 118228005
Disorder of hemostatic system 362970003
Thrombophilia 234467004
Hereditary thrombophilia 439698008
Hereditary protein C deficiency 439274008
Homozygous protein C deficiency 441188004
Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT Concept 138875005
Clinical finding 404684003
Bleeding 131148009
Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder 724854007
Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

ancestors

sorted most to least specific

Purpura fulminans 13507004
Cardiovascular system hereditary disorder 363005004
Hereditary disorder of the integument 363185004
Homozygous protein C deficiency 441188004
Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder 724854007
Acute skin disorder 127334004
Hereditary disorder by system 363137000
Hereditary protein C deficiency 439274008
Acute disease of cardiovascular system 128487001
Capillary thrombosis 17810004
Secondary non-thrombocytopenic purpura 234495004
Injury of blood vessel 57662003
Disseminated intravascular coagulation 67406007
Skin necrosis 95347000
Acute disease 2704003
Hereditary thrombophilia 439698008
Thrombosis of blood vessel 439129009
Non-thrombocytopenic purpura 234493006
Injury of integument 125592002
Protein C deficiency disease 76407009
Disorder of capillaries 58729003
Purpura simplex 277791008
Soft tissue injury 282026002
Cardiovascular injury 282728007
Necrosis of anatomical site 609410002
Hereditary disease 32895009
Thrombophilia 234467004
Purpuric disorder 387778001
Vascular disorder 27550009
Deficiency of naturally occurring coagulation factor inhibitor 105604006
Capillary finding 248723009
Thrombosis 439127006
Traumatic or non-traumatic injury 417163006
Genetic disease 782964007
Bleeding skin 297968009
Blood coagulation disorder 64779008
Disorder of cardiovascular system 49601007
Blood vessel finding 21829004
Skin lesion 95324001
Disorder of hemostatic system 362970003
Bleeding 131148009
Soft tissue lesion 239953001
Disorder of skin 95320005
Cardiovascular finding 106063007
Lesion of skin and/or skin-associated mucous membrane 714974000
Functional finding 118228005
Skin finding 106076001
Skin or mucosa lesion 247440002
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of integument 128598002
Disorder of soft tissue 19660004
Skin AND/OR mucosa finding 415531008
Integumentary system finding 106077005
General finding of soft tissue 248402002
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Acute disease 2704003

Acute skin disorder 127334004

Purpura fulminans 13507004

Neonatal purpura fulminans due to homozygous protein C deficiency 402851000

SNOMED CT code