Subcutaneous hemorrhage
Symptom Information:
Symptom ID: | HPO:0001933 | |||||||||||||||||||||||
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 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) |
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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) |