Gingival bleeding
Symptom Information:
Symptom ID: | HPO:0000225 | |||||||||||||||||||||||||
Synonyms: |
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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) Gingival bleeding(HPO:0000225) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the oral cavity(HPO:0000163) Abnormality of the gingiva(HPO:0000168) Gingival bleeding(HPO:0000225) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Gingival bleeding(HPO:0000225) |
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Database Frequency: | 28 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Attenuated Chédiak-Higashi syndrome | (Orphanet:352723) |
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT | (OMIM:153670) |
Bernard-Soulier syndrome | (Orphanet:274) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Congenital factor II deficiency | (Orphanet:325) |
Congenital factor X deficiency | (Orphanet:328) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Dengue fever | (Orphanet:99828) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
FACTOR XIII, A SUBUNIT, DEFICIENCY OF | (OMIM:613225) |
Familial afibrinogenemia | (Orphanet:98880) |
Familial dysfibrinogenemia | (Orphanet:98881) |
Familial hypofibrinogenemia | (Orphanet:101041) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Glanzmann thrombasthenia | (Orphanet:849) |
HERMANSKY-PUDLAK SYNDROME 1 | (OMIM:203300) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
INTEGRIN, BETA-3 | (OMIM:173470) |
Polycythemia vera | (Orphanet:729) |
Scleroderma | (Orphanet:801) |
Viral hemorrhagic fever | (Orphanet:341) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Wiskott-Aldrich syndrome | (Orphanet:906) |