Prolonged bleeding time

Symptom Information:

Symptom ID: HPO:0003010
Synonyms:
Increased bleeding time [HPO:0003010]
Bleeding time prolonged [Orphanet:48680]
Increased bleeding time [OMIM:Increased bleeding time]
Prolonged bleeding time [OMIM:Prolonged bleeding time]
Hemorrhage/hemorrhagic syndrome/excessive/long-lasting bleeding [Orphanet:48680]
Bleeding time prolonged [MedDRA:10005140]
Bleeding time increased [MedDRA:10005140]
Haemostasis prolonged [MedDRA:10005140]
Hemostasis prolonged [MedDRA:10005140]
Bleeding time prolonged [OMIM:Bleeding time prolonged]
Prolonged bleeding time (10 - >30 minutes) [OMIM:Prolonged bleeding time (10 - >30 minutes)]
Prolonged bleeding time (less common) [OMIM:Prolonged bleeding time (less common)]
Quality:
Cross references:
HPO:0001892 "Abnormal bleeding" [Orphanet:48680]
Orphanet:48680 "Hemorrhage/hemorrhagic syndrome/excessive/long-lasting bleeding" [Orphanet:48680]
OMIM: "Increased bleeding time" [OMIM:Increased bleeding time]
OMIM: "Prolonged bleeding time" [OMIM:Prolonged bleeding time]
OMIM: "Bleeding time prolonged" [OMIM:Bleeding time prolonged]
OMIM: "Prolonged bleeding time (10 - >30 minutes)" [OMIM:Prolonged bleeding time (10 - >30 minutes)]
OMIM: "Prolonged bleeding time (less common)" [OMIM:Prolonged bleeding time (less common)]
UMLS:C0151529 "Bleeding time prolonged" [Orphanet:48680]
Is a (Direct Parents):
MedDRA Coagulation and bleeding analyses
Orphanet Abnormal bleeding
HPO         Abnormality of thrombocytes
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)
             Prolonged bleeding time(HPO:0003010)
MedDRA:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          Prolonged bleeding time(HPO:0003010)
Database Frequency: 88 / 7739
Resource:

All diseases associated with this symptom:

ATHROMBIA, ESSENTIAL (OMIM:209050)
Alpha-thalassemia - myelodysplastic syndrome (Orphanet:231401)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Aplasia cutis - myopia (Orphanet:1117)
Aplasia cutis congenita - intestinal lymphangiectasia (Orphanet:1116)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
BERNARD-SOULIER SYNDROME (OMIM:231200)
BLEEDING DISORDER, PLATELET-TYPE, 14 (OMIM:614158)
BLEEDING DISORDER, PLATELET-TYPE, 17 (OMIM:187900)
BLEEDING DISORDER, PLATELET-TYPE, 18 (OMIM:615888)
Babesiosis (Orphanet:108)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Bleeding diathesis due to glycoprotein VI deficiency (Orphanet:98885)
Blue rubber bleb nevus (Orphanet:1059)
Choreoacanthocytosis (Orphanet:2388)
Circumscribed cutaneous aplasia of the vertex (Orphanet:1114)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital factor II deficiency (Orphanet:325)
Congenital factor V deficiency (Orphanet:326)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Deafness - lymphedema - leukemia (Orphanet:3226)
Disorder of bile acid synthesis (Orphanet:79168)
Dyskeratosis congenita (Orphanet:1775)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Enchondromatosis (Orphanet:296)
Essential thrombocythemia (Orphanet:3318)
FECHTNER SYNDROME (OMIM:153640)
Familial afibrinogenemia (Orphanet:98880)
Familial dysfibrinogenemia (Orphanet:98881)
Familial hypofibrinogenemia (Orphanet:101041)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
Familial thrombocytosis (Orphanet:71493)
Galactosemia (Orphanet:352)
Gaucher disease (Orphanet:355)
Glanzmann thrombasthenia (Orphanet:849)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Gray platelet syndrome (Orphanet:721)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hairy cell leukemia variant (Orphanet:300878)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Klippel-Trénaunay syndrome (Orphanet:90308)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MACS syndrome (Orphanet:217335)
MAY-HEGGLIN ANOMALY (OMIM:155100)
MYH9-related thrombocytopenia (Orphanet:182050)
Malakoplakia (Orphanet:556)
Marburg hemorrhagic fever (Orphanet:99826)
McCune-Albright syndrome (Orphanet:562)
Mixed connective tissue disease (Orphanet:809)
NOONAN SYNDROME 4 (OMIM:610733)
Neonatal hemochromatosis (Orphanet:446)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Noonan syndrome (Orphanet:648)
P2Y12 defect (Orphanet:36355)
PLATELET DISORDER, UNDEFINED (OMIM:173420)
PLATELET GLYCOPROTEIN IV DEFICIENCY (OMIM:608404)
Paris-Trousseau thrombocytopenia (Orphanet:851)
Parkes Weber syndrome (Orphanet:90307)
Paroxysmal cold hemoglobinuria (Orphanet:90035)
Platelet storage pool disease (Orphanet:98454)
Primary familial polycythemia (Orphanet:90042)
Pseudoxanthoma elasticum (Orphanet:758)
SEBASTIAN SYNDROME (OMIM:605249)
Scrub typhus (Orphanet:83317)
Sea-blue histiocytosis (Orphanet:158029)
TATSUMI FACTOR DEFICIENCY (OMIM:272650)
Thymic tumor (Orphanet:100100)
Tyrosinemia type 1 (Orphanet:882)
VON WILLEBRAND DISEASE, X-LINKED FORM (OMIM:314560)
Von Willebrand disease type 1 (Orphanet:166078)
Von Willebrand disease type 3 (Orphanet:166096)
Von Willebrand disease, platelet type (Orphanet:52530)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wiskott-Aldrich syndrome (Orphanet:906)
Wolfram syndrome 2 (OMIM:604928)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)