Spontaneous, recurrent epistaxis
Symptom Information:
Symptom ID: | HPO:0004406 | ||||||
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) Abnormal bleeding(HPO:0001892) Epistaxis(HPO:0000421) Spontaneous, recurrent epistaxis(HPO:0004406) 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) Spontaneous, recurrent epistaxis(HPO:0004406) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
PRIMARY RELEASE DISORDER OF PLATELETS | (OMIM:176630) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5 | (OMIM:615506) |