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86635005: Kasabach-Merritt syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Skin AND/OR mucosa finding\Skin finding\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome

\Mass of body structure\Mass of soft tissue\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Mass of body structure\Mass of body region\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome

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

\General finding of soft tissue\Mass of soft tissue\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\General finding of soft tissue\Skin finding\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome

\Functional finding\Disorder of hemostatic system\...

\Blood coagulation disorder\Kasabach-Merritt syndrome

\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia\Kasabach-Merritt syndrome

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Integumentary system finding\Skin finding\Mass of skin\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome

\Disease\Disorder of cellular component of blood\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia\Kasabach-Merritt syndrome
\Disease\Neoplasm and/or hamartoma\Angiomatosis\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Kasabach-Merritt syndrome
\Disease\Disorder of hemostatic system\Platelet disorder\Thrombocytopenic disorder\Congenital thrombocytopenia\Kasabach-Merritt syndrome
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Disease\Congenital disease\Congenital thrombocytopenia\Kasabach-Merritt syndrome
\Disease\Congenital disease\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Congenital cutaneous angiomatosis\Kasabach-Merritt syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

143679018 Kasabach-Merritt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
143680015 Thrombocytopenia-hemangioma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
507185018 Thrombocytopenia-haemangioma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
828940012 Kasabach-Merritt syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1217041012 Haemangiomatosis with thrombocytopenia en Synonym Active Entire term case insensitive SNOMED CT core module
1217042017 Haemangioma-haemorrhage syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1218529014 Hemangioma-hemorrhage syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1218530016 Hemangiomatosis with thrombocytopenia en Synonym Active Entire term case insensitive SNOMED CT core module
3036196016 Kasabach Merritt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Kasabach-Merritt syndrome	Is a	Thrombocytopenia	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Vascular disease of the skin	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital anomaly of the hematopoietic system	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Neoplasm of blood vessel	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Strawberry nevus of skin	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Associated morphology	Neoplasm, benign	false	Inferred relationship	Existential restriction modifier	3
Kasabach-Merritt syndrome	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Associated morphology	Hemangioma, no International Classification of Diseases for Oncology subtype	false	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Finding site	Blood vessel structure	false	Inferred relationship	Existential restriction modifier	4
Kasabach-Merritt syndrome	Pathological process	Neoplastic process	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Pathological process	Benign neoplastic process	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Finding site	Platelet	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Associated morphology	Vascular nevus	false	Inferred relationship	Existential restriction modifier	3
Kasabach-Merritt syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Thrombocytopenic disorder	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	4
Kasabach-Merritt syndrome	Associated morphology	Neoplasm	false	Inferred relationship	Existential restriction modifier	4
Kasabach-Merritt syndrome	Is a	Hemangioma of skin	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Hemangioma	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Hemangioendothelioma of skin	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Associated morphology	Hemangioendothelioma	false	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Associated morphology	Congenital hemangiomatosis	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital anomaly of the hematopoietic system	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Has definitional manifestation	Platelet count below reference range	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Associated morphology	Hemangioendothelioma	false	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Is a	Angiomatosis	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital anomaly of skin	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital cutaneous angiomatosis	true	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Associated morphology	Congenital hemangiomatosis	false	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Is a	Platelet disorder	false	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Blood coagulation disorder	true	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Is a	Congenital thrombocytopenia	true	Inferred relationship	Existential restriction modifier
Kasabach-Merritt syndrome	Interprets	Platelet count	true	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	1
Kasabach-Merritt syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Associated morphology	Hemangiomatosis	true	Inferred relationship	Existential restriction modifier	2
Kasabach-Merritt syndrome	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	3
Kasabach-Merritt syndrome	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
143679018	Kasabach-Merritt syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
143680015	Thrombocytopenia-hemangioma syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
507185018	Thrombocytopenia-haemangioma syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
828940012	Kasabach-Merritt syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1217041012	Haemangiomatosis with thrombocytopenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1217042017	Haemangioma-haemorrhage syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1218529014	Hemangioma-hemorrhage syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1218530016	Hemangiomatosis with thrombocytopenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3036196016	Kasabach Merritt syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module