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1208725005: Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4970633011 Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970634017 Cutaneovisceral angiomatosis, thrombocytopenia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970635016 MLT - multifocal lymphangioendotheliomatosis with thrombocytopenia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4970636015 Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5399860015 A rare lymphatic system anomaly characterized by multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract, and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically, the lesions appear as round to oval, red-brown plaques, as large as a few centimeters in diameter. Histopathologically, they consist of dilated, thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers, and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399861016 A rare lymphatic system anomaly characterised by multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract, and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically, the lesions appear as round to oval, red-brown plaques, as large as a few centimetres in diameter. Histopathologically, they consist of dilated, thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers, and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4970633011 Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970634017 Cutaneovisceral angiomatosis, thrombocytopenia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970635016 MLT - multifocal lymphangioendotheliomatosis with thrombocytopenia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4970636015 Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970637012 A rare lymphatic system anomaly with characteristics of multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically the lesions appear as round to oval red-brown plaques and as large as a few centimeters in diameter. Histopathologically they consist of dilated thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4970638019 A rare lymphatic system anomaly with characteristics of multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically the lesions appear as round to oval red-brown plaques and as large as a few centimetres in diameter. Histopathologically they consist of dilated thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399860015 A rare lymphatic system anomaly characterized by multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract, and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically, the lesions appear as round to oval, red-brown plaques, as large as a few centimeters in diameter. Histopathologically, they consist of dilated, thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers, and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399861016 A rare lymphatic system anomaly characterised by multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract, and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically, the lesions appear as round to oval, red-brown plaques, as large as a few centimetres in diameter. Histopathologically, they consist of dilated, thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers, and resembling benign lymphangioendothelioma. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3394801001000118 Multifokale Lymphangioendotheliomatose-Thrombozytopenie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3394801001000118 Multifokale Lymphangioendotheliomatose-Thrombozytopenie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Is a Lymphatic malformation true Inferred relationship Existential restriction modifier (core metadata concept)
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Is a Finding of lymph node and lymphatics true Inferred relationship Existential restriction modifier (core metadata concept)
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Is a Congenital thrombocytopaenia true Inferred relationship Existential restriction modifier (core metadata concept)
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 3
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Finding site Structure of lymphatic vessel true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Associated morphology Congenital lymphatic malformation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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