Subcutaneous hemorrhage

Symptom Information:

Symptom ID: HPO:0001933
Synonyms:
Cutaneous hemorrhage [Orphanet:48820]
Bleeding skin (finding) [Orphanet:48820]
Skin hemorrhages [Orphanet:48820]
Bleeding skin [Orphanet:48820]
Haemorrhage subcutaneous [Orphanet:48820]
Mucosal/cutaneous hemorrhage [Orphanet:48820]
Skin bleeding [Orphanet:48820]
Skin haemorrhage [Orphanet:48820]
Skin haemorrhage [MedDRA:10064265]
Skin necrosis haemorrhagic [MedDRA:10064265]
Skin necrosis hemorrhagic [MedDRA:10064265]
Skin bleeding [MedDRA:10064265]
Skin hemorrhage [MedDRA:10064265]
Haemorrhage subcutaneous [MedDRA:10018999]
Bleeding spot subcutaneous [MedDRA:10018999]
Hemorrhage subcutaneous [MedDRA:10018999]
Vibices [MedDRA:10018999]
Subcutaneous bleeding [MedDRA:10018999]
Subcutaneous bleeding [OMIM:Subcutaneous bleeding]
Mucosal haemorrhage [MedDRA:10061298]
Mucosal hemorrhage [Orphanet:48820]
Mucosal haemorrhage [Orphanet:48820]
Skin haemorrhages [MedDRA:10040860]
Quality:
Cross references:
Orphanet:48820 "Mucosal/cutaneous hemorrhage" [Orphanet:48820]
OMIM: "Subcutaneous bleeding" [OMIM:Subcutaneous bleeding]
UMLS:C0852361 "Skin hemorrhages" [Orphanet:48820]
UMLS:C0574741 "Bleeding skin" [Orphanet:48820]
UMLS:C0854107 "Haemorrhage subcutaneous" [Orphanet:48820]
UMLS:C0854375 "Mucosal haemorrhage" [Orphanet:48820]
Is a (Direct Parents):
Orphanet Abnormal bleeding
MedDRA Vascular skin abnormality
HPO         Abnormal bleeding
HPO         Vascular skin abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Vascular skin abnormality(HPO:0011276)
                   Subcutaneous hemorrhage(HPO:0001933)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Subcutaneous hemorrhage(HPO:0001933)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Vascular skin abnormality(HPO:0011276)
       Subcutaneous hemorrhage(HPO:0001933)
Database Frequency: 50 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Anti-glomerular basement membrane disease (Orphanet:375)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
Blau syndrome (Orphanet:90340)
CADASIL (Orphanet:136)
CINCA syndrome (Orphanet:1451)
Castleman disease (Orphanet:160)
Classical homocystinuria (Orphanet:394)
Cogan syndrome (Orphanet:1467)
Common variable immunodeficiency (Orphanet:1572)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Dengue fever (Orphanet:99828)
Diffuse cutaneous mastocytosis (Orphanet:79456)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
FACTOR XIII, A SUBUNIT, DEFICIENCY OF (OMIM:613225)
Familial cold urticaria (Orphanet:47045)
Gamma heavy-chain disease (Orphanet:100026)
Gaucher disease type 2 (Orphanet:77260)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Granulomatosis with polyangiitis (Orphanet:900)
Griscelli disease type 2 (Orphanet:79477)
Hereditary thrombophilia due to congenital protein C deficiency (Orphanet:745)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Immunoglobulin A vasculitis (Orphanet:761)
Junctional epidermolysis bullosa (Orphanet:305)
Microscopic polyangiitis (Orphanet:727)
Mixed connective tissue disease (Orphanet:809)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Osteogenesis imperfecta (Orphanet:666)
Osteopetrosis (Orphanet:2781)
PTEN hamartoma tumor syndrome (Orphanet:306498)
Polyarteritis nodosa (Orphanet:767)
Relapsing polychondritis (Orphanet:728)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Rift valley fever (Orphanet:319251)
Sea-blue histiocytosis (Orphanet:158029)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
Viral hemorrhagic fever (Orphanet:341)
Waldenström macroglobulinemia (Orphanet:33226)
Wiskott-Aldrich syndrome (Orphanet:906)