Abnormal bleeding
Symptom Information:
Symptom ID: | HPO:0001892 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Abnormal bleeding(HPO:0001892) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Coagulation and bleeding analyses(MedDRA:10009728) Abnormal bleeding(HPO:0001892) Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Haemorrhages NEC(MedDRA:10018987) Abnormal bleeding(HPO:0001892) |
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Database Frequency: | 85 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADENOMYOSIS | (OMIM:600458) |
ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO | (OMIM:207300) |
ATHROMBIA, ESSENTIAL | (OMIM:209050) |
Acid phosphatase deficiency | (Orphanet:35121) |
Aplasia cutis congenita - intestinal lymphangiectasia | (Orphanet:1116) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
BERNARD-SOULIER SYNDROME | (OMIM:231200) |
BLEEDING DISORDER, PLATELET-TYPE, 14 | (OMIM:614158) |
BLEEDING DISORDER, PLATELET-TYPE, 17 | (OMIM:187900) |
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency | (Orphanet:91135) |
CAR FACTOR DEFICIENCY | (OMIM:114650) |
Combined deficiency of factor V and factor VIII | (Orphanet:35909) |
Congenital alpha2 antiplasmin deficiency | (Orphanet:79) |
Congenital factor V deficiency | (Orphanet:326) |
Congenital factor VII deficiency | (Orphanet:327) |
Congenital factor X deficiency | (Orphanet:328) |
Congenital factor XI deficiency | (Orphanet:329) |
DK1-CDG | (Orphanet:91131) |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 | (OMIM:227300) |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR | (OMIM:227310) |
FACTOR VIII DEFICIENCY | (OMIM:134500) |
FACTOR XIII, A SUBUNIT, DEFICIENCY OF | (OMIM:613225) |
FACTOR XIII, B SUBUNIT, DEFICIENCY OF | (OMIM:613235) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FECHTNER SYNDROME | (OMIM:153640) |
FIBRINOLYTIC DEFECT | (OMIM:134900) |
Familial acute necrotizing encephalopathy | (Orphanet:88619) |
Fetal Gaucher disease | (Orphanet:85212) |
GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN | (OMIM:137900) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
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) |
HYPERHEPARINEMIA | (OMIM:144050) |
Hemophilia A | (Orphanet:98878) |
Hemophilia B | (Orphanet:98879) |
Hereditary combined deficiency of vitamin K-dependent clotting factors | (Orphanet:98434) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
Hermansky-Pudlak syndrome without pulmonary fibrosis | (Orphanet:231512) |
Immune thrombocytopenic purpura | (Orphanet:3002) |
Leukocyte adhesion deficiency type III | (Orphanet:99844) |
MEGDEL syndrome | (Orphanet:352328) |
MPI-CDG | (Orphanet:79319) |
MYH9-related thrombocytopenia | (Orphanet:182050) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Neonatal hemochromatosis | (Orphanet:446) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
P2Y12 defect | (Orphanet:36355) |
PASSOVOY FACTOR DEFECT | (OMIM:168830) |
PECHET FACTOR DEFICIENCY | (OMIM:169200) |
PEROXISOME BIOGENESIS DISORDER 3B | (OMIM:266510) |
PLATELET DISORDER, UNDEFINED | (OMIM:173420) |
PLATELET FACTOR 3 DEFICIENCY | (OMIM:173450) |
PLATELET GLYCOPROTEIN IV DEFICIENCY | (OMIM:608404) |
PLATELET SIGNAL PROCESSING DEFECT | (OMIM:173590) |
Paris-Trousseau thrombocytopenia | (Orphanet:851) |
Platelet storage pool disease | (Orphanet:98454) |
SLC35A2-CDG | (Orphanet:356961) |
SRD5A3-CDG | (Orphanet:324737) |
Scott syndrome | (Orphanet:806) |
Sitosterolemia | (Orphanet:2882) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
TATSUMI FACTOR DEFICIENCY | (OMIM:272650) |
THROMBOCYTOPENIA 3 | (OMIM:273900) |
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE | (OMIM:314000) |
THROMBOCYTOPENIA, CYCLIC | (OMIM:188020) |
Transaldolase deficiency | (Orphanet:101028) |
Tyrosinemia type 1 | (Orphanet:882) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 | (OMIM:607473) |
VON WILLEBRAND DISEASE, X-LINKED FORM | (OMIM:314560) |
WISKOTT-ALDRICH SYNDROME | (OMIM:277970) |
Wolfram syndrome 2 | (OMIM:604928) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |