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1187614006: Severe autosomal recessive macrothrombocytopenia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4674355015 Severe autosomal recessive macrothrombocytopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674356019 Severe autosomal recessive macrothrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5399654018 A rare isolated hereditary giant platelet disorder characterized by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestation are recurrent bleeding episodes including epistaxis, spontaneous hematoma, and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399655017 A rare isolated hereditary giant platelet disorder characterised by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestation are recurrent bleeding episodes including epistaxis, spontaneous haematoma, and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674355015 Severe autosomal recessive macrothrombocytopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674356019 Severe autosomal recessive macrothrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674357011 A rare isolated hereditary giant platelet disorder characterised by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestations are recurrent bleeding episodes including epistaxis, spontaneous haematoma and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674358018 A rare isolated hereditary giant platelet disorder characterized by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestations are recurrent bleeding episodes including epistaxis, spontaneous hematoma and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399654018 A rare isolated hereditary giant platelet disorder characterized by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestation are recurrent bleeding episodes including epistaxis, spontaneous hematoma, and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399655017 A rare isolated hereditary giant platelet disorder characterised by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestation are recurrent bleeding episodes including epistaxis, spontaneous haematoma, and menorrhagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3415261001000114 Makrothrombozytopenie, schwere, autosomal-rezessive de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415261001000114 Makrothrombozytopenie, schwere, autosomal-rezessive 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
Severe autosomal recessive macrothrombocytopenia (disorder) Is a Giant platelet syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Severe autosomal recessive macrothrombocytopenia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Severe autosomal recessive macrothrombocytopenia (disorder) Finding site Body system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe autosomal recessive macrothrombocytopenia (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe autosomal recessive macrothrombocytopenia (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe autosomal recessive macrothrombocytopenia (disorder) Is a Hereditary platelet function disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Severe autosomal recessive macrothrombocytopenia (disorder) Is a Hereditary thrombocytopenic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Severe autosomal recessive macrothrombocytopenia (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 3
Severe autosomal recessive macrothrombocytopenia (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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