Impaired platelet aggregation
Symptom Information:
Symptom ID: | HPO:0003540 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of thrombocytes(HPO:0001872) Abnormal platelet function(HPO:0011869) Impaired platelet aggregation(HPO:0003540) MedDRA: Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Platelet analyses(MedDRA:10035523) Impaired platelet aggregation(HPO:0003540) |
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Database Frequency: | 17 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
ATHROMBIA, ESSENTIAL | (OMIM:209050) |
Autosomal dominant macrothrombocytopenia | (Orphanet:140957) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
BLEEDING DISORDER, PLATELET-TYPE, 12 | (OMIM:605735) |
Bartter syndrome | (Orphanet:112) |
Essential thrombocythemia | (Orphanet:3318) |
Familial platelet syndrome with predisposition to acute myelogenous leukemia | (Orphanet:71290) |
Glanzmann thrombasthenia | (Orphanet:849) |
Hermansky-Pudlak syndrome type 7 | (Orphanet:231531) |
INTEGRIN, BETA-3 | (OMIM:173470) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
PLATELET DISORDER, UNDEFINED | (OMIM:173420) |
Sitosterolemia | (Orphanet:2882) |
Transaldolase deficiency | (Orphanet:101028) |
Von Willebrand disease type 1 | (Orphanet:166078) |
Von Willebrand disease type 3 | (Orphanet:166096) |
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia | (Orphanet:363727) |