Joint hemorrhage

Symptom Information:

Symptom ID: HPO:0005261
Synonyms:
Hemarthroses [HPO:0005261]
Hemarthrosis [HPO:0005261]
Joint haemorrhage [HPO:0005261]
Spontaneous joint hemorrhage [HPO:0005261]
Hemarthrosis [Orphanet:48720]
Hemarthrosis (disorder) [Orphanet:48720]
Hemarthroses [OMIM:Hemarthroses]
Hemarthrosis [OMIM:Hemarthrosis]
Spontaneous joint hemorrhage [OMIM:Spontaneous joint hemorrhage]
Haemarthrosis [Orphanet:48720]
Haemarthrosis [MedDRA:10018829]
Hemarthrosis involving upper arm [MedDRA:10018829]
Hemarthrosis [MedDRA:10018829]
Hemarthrosis involving ankle and foot [MedDRA:10018829]
Hemarthrosis involving forearm [MedDRA:10018829]
Hemarthrosis involving hand [MedDRA:10018829]
Hemarthrosis involving lower leg [MedDRA:10018829]
Hemarthrosis involving multiple sites [MedDRA:10018829]
Hemarthrosis involving other specified sites [MedDRA:10018829]
Hemarthrosis involving pelvic region and thigh [MedDRA:10018829]
Hemarthrosis, site unspecified [MedDRA:10018829]
Herarthrosis involving shoulder region [MedDRA:10018829]
Intraarticular haemorrhage [MedDRA:10018829]
Intraarticular hemorrhage [MedDRA:10018829]
Joint bleeding [MedDRA:10018829]
Haemarthrosis involving forearm [MedDRA:10018829]
Haemarthrosis involving hand [MedDRA:10018829]
Haemarthrosis involving lower leg [MedDRA:10018829]
Haemarthrosis involving upper arm [MedDRA:10018829]
Haemarthrosis, site unspecified [MedDRA:10018829]
Joint haematoma [MedDRA:10018829]
Joint hematoma [MedDRA:10018829]
Quality:
Cross references:
Orphanet:48720 "Hemarthrosis" [Orphanet:48720]
OMIM: "Hemarthroses" [OMIM:Hemarthroses]
OMIM: "Hemarthrosis" [OMIM:Hemarthrosis]
OMIM: "Spontaneous joint hemorrhage" [OMIM:Spontaneous joint hemorrhage]
UMLS:C0018924 "Hemarthroses" [HPO:0005261]
UMLS:C0018924 "Hemarthrosis" [Orphanet:48720]
Is a (Direct Parents):
Orphanet Abnormal bleeding
HPO         Abnormal joint morphology
HPO         Internal hemorrhage
MedDRA Limb injuries NEC (incl traumatic amputation)
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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 blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             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)
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)