Epistaxis
Symptom Information:
Symptom ID: | HPO:0000421 | |||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||
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 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) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) 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) |
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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) |