Epistaxis

Symptom Information:

Symptom ID: HPO:0000421
Synonyms:
nose bleeding [HPO:0000421]
nosebleed [HPO:0000421]
Epistaxis (disorder) [Orphanet:48740]
Bleeding from nose (finding) [Orphanet:48740]
epistaxis [HPO:0000421]
Epistaxis [Orphanet:48740]
Epistaxis [OMIM:Epistaxis]
Epistaxis/nose bleeding [Orphanet:48740]
Epistaxis [MedDRA:10015090]
Bleeding nose [MedDRA:10015090]
Haemorrhage nasal [MedDRA:10015090]
Hemorrhage nasal [MedDRA:10015090]
Nasal bleeding [MedDRA:10015090]
Nasal mucus blood tinged [MedDRA:10015090]
Nose bleed [MedDRA:10015090]
Nose bleeds [MedDRA:10015090]
Nosebleed [MedDRA:10015090]
Chronic epistaxis [MedDRA:10015090]
Epistaxis (in some patients) [OMIM:Epistaxis (in some patients)]
Quality:
Cross references:
Orphanet:48740 "Epistaxis/nose bleeding" [Orphanet:48740]
OMIM: "Epistaxis" [OMIM:Epistaxis]
OMIM: "Epistaxis (in some patients)" [OMIM:Epistaxis (in some patients)]
UMLS:C2228238 "epistaxis" [HPO:0000421]
UMLS:C0014591 "Epistaxis" [Orphanet:48740]
Is a (Direct Parents):
HPO         Abnormality of the nose
Orphanet Abnormal bleeding
HPO         Abnormal bleeding
MedDRA Nasal disorders NEC
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)
             Epistaxis(HPO:0000421)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Epistaxis(HPO:0000421)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Upper respiratory tract disorders (excl infections)(MedDRA:10046304)
       Nasal disorders NEC(MedDRA:10028731)
          Epistaxis(HPO:0000421)
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
BERNARD-SOULIER SYNDROME (OMIM:231200)
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
BLEEDING DISORDER, PLATELET-TYPE, 12 (OMIM:605735)
BLEEDING DISORDER, PLATELET-TYPE, 14 (OMIM:614158)
BLEEDING DISORDER, PLATELET-TYPE, 15 (OMIM:615193)
BLEEDING DISORDER, PLATELET-TYPE, 17 (OMIM:187900)
BLEEDING DISORDER, PLATELET-TYPE, 18 (OMIM:615888)
BLEEDING DISORDER, PLATELET-TYPE, 19 (OMIM:616176)
Bernard-Soulier syndrome (Orphanet:274)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Bleeding diathesis due to glycoprotein VI deficiency (Orphanet:98885)
Bleeding diathesis due to thromboxane synthesis deficiency (Orphanet:220443)
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency (Orphanet:91135)
Chédiak-Higashi syndrome (Orphanet:167)
Congenital factor II deficiency (Orphanet:325)
Congenital factor V deficiency (Orphanet:326)
Congenital factor VII deficiency (Orphanet:327)
Congenital factor X deficiency (Orphanet:328)
Congenital factor XIII deficiency (Orphanet:331)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Dengue fever (Orphanet:99828)
EPISTAXIS, HEREDITARY (OMIM:132500)
EPSTEIN SYNDROME (OMIM:153650)
Ebola hemorrhagic fever (Orphanet:319218)
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 (OMIM:613625)
FACTOR XIII, A SUBUNIT, DEFICIENCY OF (OMIM:613225)
Familial afibrinogenemia (Orphanet:98880)
Familial dysfibrinogenemia (Orphanet:98881)
Familial hypofibrinogenemia (Orphanet:101041)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Giant cell arteritis (Orphanet:397)
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)
Granulomatosis with polyangiitis (Orphanet:900)
Gray platelet syndrome (Orphanet:721)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
HERMANSKY-PUDLAK SYNDROME 6 (OMIM:614075)
Hereditary North American Indian childhood cirrhosis (Orphanet:168583)
Hereditary combined deficiency of vitamin K-dependent clotting factors (Orphanet:98434)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome type 7 (Orphanet:231531)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
INTEGRIN, BETA-3 (OMIM:173470)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Leukocyte adhesion deficiency type III (Orphanet:99844)
MAY-HEGGLIN ANOMALY (OMIM:155100)
Microscopic polyangiitis (Orphanet:727)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
P2Y12 defect (Orphanet:36355)
PASSOVOY FACTOR DEFECT (OMIM:168830)
PLATELET SIGNAL PROCESSING DEFECT (OMIM:173590)
PURPURA SIMPLEX (OMIM:179000)
Polycythemia vera (Orphanet:729)
Primary familial polycythemia (Orphanet:90042)
Primary localized amyloidosis (Orphanet:314709)
Quebec platelet disorder (Orphanet:220436)
Rheumatic fever (Orphanet:3099)
SEBASTIAN SYNDROME (OMIM:605249)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
THROMBOCYTOPENIA 5 (OMIM:616216)
Thrombocytopenia with congenital dyserythropoietic anemia (Orphanet:67044)
Transaldolase deficiency (Orphanet:101028)
Typhoid (Orphanet:99745)
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 (OMIM:277450)
Viral hemorrhagic fever (Orphanet:341)
Von Willebrand disease type 1 (Orphanet:166078)
Von Willebrand disease type 2 (Orphanet:166081)
Von Willebrand disease type 2A (Orphanet:166084)
Von Willebrand disease type 2B (Orphanet:166087)
Von Willebrand disease type 2M (Orphanet:166090)
Von Willebrand disease type 2N (Orphanet:166093)
Von Willebrand disease type 3 (Orphanet:166096)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Waldenström macroglobulinemia (Orphanet:33226)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked thrombocytopenia with normal platelets (Orphanet:852)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)