CPT Changes Current book and archives back to 2000 Easy-to-read online book format Linked to and from code details
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Hereditary platelet function disorder 128096008 SNOMED CT code SNOMED code 128096008 name Hereditary platelet function disorder status active date introduced 2002-01-31 fully specified name(s) Hereditary platelet function disorder (disorder) synonyms Hereditary platelet function disorder attributes - group1 Interprets Hemostatic function 74848003 Has interpretation Abnormal 263654008 attributes - group2 Finding site Body system structure 91689009 parents children Bernard Soulier syndrome 54569005 Bleeding diathesis due to collagen receptor defect 782934004 Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency 725105006 Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 1172901009 Defect of purinergic receptor p2y G protein-coupled 12 725291001 Familial alpha>2< adrenergic receptor defect in platelets 128102001 Glanzmann's thrombasthenia 32942005 Isolated collagen aggregation defect 128103006 Platelet procoagulant activity deficiency 43346008 Platelet secretory disorder 51448009 Platelet storage pool defect 128099001 Platelet type pseudo-von Willebrand disease 270117002 removed: 2022-11-30 Pseudo von Willebrand disease 128115005 Scott syndrome 128098009 Severe autosomal recessive macrothrombocytopenia 1187614006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 118228005 362970003 22716005 234469001 128096008 138875005 404684003 118228005 362970003 22716005 267532001 128096008 ancestors sorted most to least specific
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