Prolonged bleeding time
Symptom Information:
Symptom ID: | HPO:0003010 | ||||||||||||
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) 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) |
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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) |