Joint hemorrhage
Symptom Information:
Symptom ID: | HPO:0005261 | ||||||||||||||||||||||||||||||||
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) Internal hemorrhage(HPO:0011029) Joint hemorrhage(HPO:0005261) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Abnormality of blood circulation(HPO:0011028) Internal hemorrhage(HPO:0011029) Joint hemorrhage(HPO:0005261) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Joint hemorrhage(HPO:0005261) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Bone and joint injuries(MedDRA:10005942) Limb injuries NEC (incl traumatic amputation)(MedDRA:10027686) Joint hemorrhage(HPO:0005261) |
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Database Frequency: | 17 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
BLEEDING DISORDER, PLATELET-TYPE, 12 | (OMIM:605735) |
Congenital alpha2 antiplasmin deficiency | (Orphanet:79) |
Congenital factor II deficiency | (Orphanet:325) |
Congenital factor VII deficiency | (Orphanet:327) |
Congenital factor X deficiency | (Orphanet:328) |
Congenital factor XIII deficiency | (Orphanet:331) |
FACTOR XIII, A SUBUNIT, DEFICIENCY OF | (OMIM:613225) |
FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF | (OMIM:134520) |
HEMOPHILIA A | (OMIM:306700) |
HEMOPHILIA A WITH VASCULAR ABNORMALITY | (OMIM:306800) |
Hemophilia B | (Orphanet:98879) |
Hereditary combined deficiency of vitamin K-dependent clotting factors | (Orphanet:98434) |
Quebec platelet disorder | (Orphanet:220436) |
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 | (OMIM:277450) |
Von Willebrand disease type 1 | (Orphanet:166078) |
Von Willebrand disease type 3 | (Orphanet:166096) |
X-linked thrombocytopenia with normal platelets | (Orphanet:852) |