Impaired platelet aggregation

Symptom Information:

Symptom ID: HPO:0003540
Synonyms:
Abnormal platelet aggregation [HPO:0003540]
Defective platelet aggregation [HPO:0003540]
Deficient platelet aggregation [HPO:0003540]
Platelet aggregation defect [HPO:0003540]
Abnormal platelet aggregation [OMIM:Abnormal platelet aggregation]
Impaired platelet aggregation [OMIM:Impaired platelet aggregation]
Platelet aggregation defect [OMIM:Platelet aggregation defect]
Impaired platelet aggregation (in some patients) [OMIM:Impaired platelet aggregation (in some patients)]
Platelet aggregation abnormal [MedDRA:10061601]
Quality:
Cross references:
OMIM: "Abnormal platelet aggregation" [OMIM:Abnormal platelet aggregation]
OMIM: "Impaired platelet aggregation" [OMIM:Impaired platelet aggregation]
OMIM: "Platelet aggregation defect" [OMIM:Platelet aggregation defect]
OMIM: "Impaired platelet aggregation (in some patients)" [OMIM:Impaired platelet aggregation (in some patients)]
Is a (Direct Parents):
HPO         Abnormal platelet function
MedDRA Platelet analyses
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)
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)