Purpura
Symptom Information:
Symptom ID: | HPO:0000979 | ||||||||||||||||||||||||||
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) Purpura(HPO:0000979) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Subcutaneous hemorrhage(HPO:0001933) Purpura(HPO:0000979) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Purpura(HPO:0000979) Skin and subcutaneous tissue disorders(MedDRA:10040785) Vascular skin abnormality(HPO:0011276) Purpura and related conditions(MedDRA:10037555) Purpura(HPO:0000979) |
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Database Frequency: | 27 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AL amyloidosis | (Orphanet:85443) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
BERNARD-SOULIER SYNDROME | (OMIM:231200) |
COMPLEMENT COMPONENT 2 DEFICIENCY | (OMIM:217000) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fetal Gaucher disease | (Orphanet:85212) |
Gaucher disease type 2 | (Orphanet:77260) |
Glanzmann thrombasthenia | (Orphanet:849) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
IMMUNODEFICIENCY, COMMON VARIABLE, 6 | (OMIM:613496) |
INTEGRIN, BETA-3 | (OMIM:173470) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
MELAS | (Orphanet:550) |
PURPURA SIMPLEX | (OMIM:179000) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary systemic amyloidosis | (Orphanet:314701) |
Protein S acquired deficiency | (Orphanet:26349) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:612304) |
WISKOTT-ALDRICH SYNDROME | (OMIM:277970) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
Wiskott-Aldrich syndrome | (Orphanet:906) |