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737221003: Congenital thrombocytopenia (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Platelet count outside reference range\Platelet count below reference range\Thrombocytopenic disorder\Congenital thrombocytopenia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Platelet count below reference range\Thrombocytopenic disorder\Congenital thrombocytopenia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Platelet count below reference range\Thrombocytopenic disorder\Congenital thrombocytopenia
\Evaluation finding\Measurement finding\Finding of platelet count\Platelet count outside reference range\Platelet count below reference range\Thrombocytopenic disorder\Congenital thrombocytopenia
\Evaluation finding\Hematopoietic system finding\Hemostatic system finding\Finding of platelet count\Platelet count outside reference range\Platelet count below reference range\Thrombocytopenic disorder\Congenital thrombocytopenia

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia

\Functional finding\Disorder of hemostatic system\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia

\Disease\Disorder of cellular component of blood\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia
\Disease\Disorder of hemostatic system\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia
\Disease\Congenital disease\Congenital thrombocytopenia

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3527197016 Congenital thrombocytopenia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3527198014 Congenital thrombocytopenia en Synonym Active Entire term case insensitive SNOMED CT core module

3527199018 Congenital thrombocytopaenia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital thrombocytopenia	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier
Congenital thrombocytopenia	Is a	Thrombocytopenic disorder	true	Inferred relationship	Existential restriction modifier
Congenital thrombocytopenia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Congenital thrombocytopenia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Congenital thrombocytopenia	Interprets	Platelet count	true	Inferred relationship	Existential restriction modifier	2
Congenital thrombocytopenia	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	3
Congenital thrombocytopenia	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	3
Congenital thrombocytopenia	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fanconi's anemia	Is a	False	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Wiskott-Aldrich syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Radial aplasia-thrombocytopenia syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Congenital thrombocytopenic purpura	Is a	False	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Amegakaryocytic thrombocytopenia with congenital malformation	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Thrombocytopathy, asplenia and miosis	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Congenital amegakaryocytic thrombocytopenia	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
DK phocomelia syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Autosomal dominant macrothrombocytopenia	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
X-linked congenital dyserythropoietic anemia with thrombocytopenia	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Thyrocerebrorenal syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Constitutional aplastic anemia	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Bleeding diathesis due to thromboxane synthesis deficiency	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Congenital autosomal recessive small-platelet thrombocytopenia	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier
Myosin heavy chain 9 non muscle related disease	Is a	True	Congenital thrombocytopenia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3527197016	Congenital thrombocytopenia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3527198014	Congenital thrombocytopenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3527199018	Congenital thrombocytopaenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module