Abnormality of coagulation

Symptom Information:

Symptom ID: HPO:0001928
Abnormal blood coagulation studies [HPO:0001928]
Blood coagulation disorder [HPO:0001928]
Coagulation abnormalities [HPO:0001928]
Coagulation abnormality [HPO:0001928]
Haemorrhagic disorders [HPO:0001928]
Hemostasis disorder [Orphanet:48660]
Blood coagulation disorder (disorder) [Orphanet:48660]
Tendency to bleed (observable entity) [Orphanet:48660]
Disorder of hemostatic system (disorder) [Orphanet:48660]
Blood Coagulation Disorders [Orphanet:48660]
Bleeding tendency [Orphanet:48660]
Coagulation abnormalities [OMIM:Coagulation abnormalities]
Clotting/hemostasis disorders [Orphanet:48660]
Coagulopathy [Orphanet:48660]
Coagulopathy [MedDRA:10009802]
Clotting [MedDRA:10009802]
Coagulation abnormal [MedDRA:10009802]
Coagulation defects [MedDRA:10009802]
Coagulation defects, other and unspecified [MedDRA:10009802]
Coagulation disorder [MedDRA:10009802]
Coagulation disorder NOS [MedDRA:10009802]
Defect coagulation (NOS) [MedDRA:10009802]
Disorder coagulation [MedDRA:10009802]
Other and unspecified coagulation defects [MedDRA:10009802]
Postpartum coagulation defects [MedDRA:10009802]
Postpartum coagulation defects, postpartum [MedDRA:10009802]
Postpartum coagulation defects, unspecified as to episode of care [MedDRA:10009802]
Postpartum coagulation defects, with delivery [MedDRA:10009802]
Coagulation disorder (NOS) [MedDRA:10009802]
Clotting disorder [MedDRA:10009802]
Acute coagulopathy [MedDRA:10009802]
Haemorrhagic diathesis [MedDRA:10062713]
Bleeding tendency [MedDRA:10062713]
Hemorrhagic diathesis [MedDRA:10062713]
Aggravated bleeding tendency [MedDRA:10062713]
Abnormal blood coagulation studies (prolonged PT and PTT) [OMIM:Abnormal blood coagulation studies (prolonged PT and PTT)]
Bleeding tendencies [OMIM:Bleeding tendencies]
Bleeding tendency (e.g., epistaxis) [OMIM:Bleeding tendency (e.g., epistaxis)]
Coagulation defect [OMIM:Coagulation defect]
Coagulation defects [OMIM:Coagulation defects]
Coagulation defects (1 patient) [OMIM:Coagulation defects (1 patient)]
Coagulopathy (INR = 2.2 - 3.5) [OMIM:Coagulopathy (INR = 2.2 - 3.5)]
Bleeding tendencies [MedDRA:10005133]
Coagulopathies [MedDRA:10053567]
Haemorrhagic disorder [MedDRA:10019009]
Cross references:
HPO:0001892 "Abnormal bleeding" [Orphanet:48660]
Orphanet:48660 "Clotting/hemostasis disorders" [Orphanet:48660]
OMIM: "Coagulation abnormalities" [OMIM:Coagulation abnormalities]
OMIM: "Abnormal blood coagulation studies (prolonged PT and PTT)" [OMIM:Abnormal blood coagulation studies (prolonged PT and PTT)]
OMIM: "Bleeding tendencies" [OMIM:Bleeding tendencies]
OMIM: "Bleeding tendency (e.g., epistaxis)" [OMIM:Bleeding tendency (e.g., epistaxis)]
OMIM: "Coagulation defect" [OMIM:Coagulation defect]
OMIM: "Coagulation defects" [OMIM:Coagulation defects]
OMIM: "Coagulation defects (1 patient)" [OMIM:Coagulation defects (1 patient)]
OMIM: "Coagulopathy (INR = 2.2 - 3.5)" [OMIM:Coagulopathy (INR = 2.2 - 3.5)]
UMLS:C0005779 "Blood Coagulation Disorders" [Orphanet:48660]
UMLS:C1458140 "Bleeding tendency" [Orphanet:48660]
Is a (Direct Parents):
MedDRA Coagulopathies and bleeding diatheses (excl thrombocytopenic)
HPO         Abnormality of blood and blood-forming tissues
MedDRA Haemorrhages NEC
Orphanet Abnormality of blood and blood-forming tissues
MedDRA Abnormal bleeding
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of coagulation(HPO:0001928)
Blood and lymphatic system disorders(MedDRA:10005329)
    Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477)
       Abnormal bleeding(HPO:0001892)
          Abnormality of coagulation(HPO:0001928)
       Abnormality of coagulation(HPO:0001928)
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Haemorrhages NEC(MedDRA:10018987)
          Abnormal bleeding(HPO:0001892)
             Abnormality of coagulation(HPO:0001928)
          Abnormality of coagulation(HPO:0001928)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          Abnormal bleeding(HPO:0001892)
             Abnormality of coagulation(HPO:0001928)
Database Frequency: 44 / 7739

All diseases associated with this symptom:

ALG2-CDG (Orphanet:79326)
Argininemia (Orphanet:90)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
B4GALT1-CDG (Orphanet:79332)
Blue rubber bleb nevus (Orphanet:1059)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital disorder of glycosylation (Orphanet:137)
DK1-CDG (Orphanet:91131)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Dubin-Johnson syndrome (Orphanet:234)
Facial dysmorphism - shawl scrotum - joint laxity (Orphanet:1778)
Fetal Gaucher disease (Orphanet:85212)
Fetal cytomegalovirus syndrome (Orphanet:294)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Indomethacin embryofetopathy (Orphanet:1909)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
MEGDEL syndrome (Orphanet:352328)
Malignant peritoneal mesothelioma (Orphanet:168811)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Multiple sclerosis - ichthyosis - factor VIII deficiency (Orphanet:3151)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Progressive familial intrahepatic cholestasis (Orphanet:172)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
SLC35A2-CDG (Orphanet:356961)
SRD5A3-CDG (Orphanet:324737)
Sitosterolemia (Orphanet:2882)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
Thrombocytopenia - absent radius (Orphanet:3320)
Transaldolase deficiency (Orphanet:101028)
Tyrosinemia type 1 (Orphanet:882)
Von Willebrand disease (Orphanet:903)
Wilson disease (Orphanet:905)
Wolfram syndrome 2 (OMIM:604928)
Zellweger syndrome (Orphanet:912)