Disease Browser
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Parent Node: Blood Platelet Disorders (D001791) | ..Starting node ..Platelet Aggregation, Spontaneous (C566800)
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Sister Nodes: | ..Bernard-Soulier Syndrome (D001606) 5
| ..BLEEDING DISORDER, PLATELET-TYPE, 8 (OMIM:609821)
| ..Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality (C565600)
| ..Gray Platelet Syndrome (D055652) 1
| ..Platelet Aggregation, Spontaneous (C566800)
| ..Platelet Disorder, Familial, with Associated Myeloid Malignancy (C563324)
| ..Platelet Disorder, Undefined (C566799)
| ..Platelet Factor 3 Deficiency (C566798)
| ..Platelet Glycoprotein IV Deficiency (C564245)
| ..Platelet Prostacyclin Receptor Defect (C564884)
| ..Platelet Receptor for Collagen, Deficiency of (C565999)
| ..Platelet Signal Processing Defect (C566796)
| ..Platelet Storage Pool Deficiency (D010981) 5
| ..Primary Release Disorder Of Platelets (C566759)
| ..Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet (C567786)
| ..Stormorken Syndrome (C566108)
| ..Thrombasthenia (D013915) 3
| ..Thrombocytopenia (D013921) 48
| ..Thrombocytosis (D013922) 4
| ..Thromboxane Synthetase Deficiency (C562866)
| ..von Willebrand Diseases (D014842) 6
| ..White platelet syndrome (C536702)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 8992 |
Name: | Platelet Aggregation, Spontaneous |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D001791 |
TreeNumbers: | C15.378.140/C566800 |
Synonyms: | |
Slim Mappings: | Blood disease |
Reference: |
MedGen: C566800
MeSH: C566800
OMIM: 173400;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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