Purpura

Symptom Information:

Symptom ID: HPO:0000979
Synonyms:
Skin purpura [Orphanet:23610]
Purpura (finding) [Orphanet:23610]
Purpuric disorder (disorder) [Orphanet:23610]
Purpura [Orphanet:23610]
Purpura [OMIM:Purpura]
Purpura/petichiae [Orphanet:23610]
Purpura [MedDRA:10037549]
Dermatitis haemorrhagic [MedDRA:10037549]
Dermatitis hemorrhagic [MedDRA:10037549]
Haemolytic type rash [MedDRA:10037549]
Haemorrhage purpuric [MedDRA:10037549]
Idiopathic purpura [MedDRA:10037549]
Purpura NOS [MedDRA:10037549]
Purpuric rash [MedDRA:10037549]
Rash haemorrhagic [MedDRA:10037549]
Rash hemorrhagic [MedDRA:10037549]
Rash purpitic [MedDRA:10037549]
Rash purpuric [MedDRA:10037549]
Purpura symptomatica [MedDRA:10037549]
Hemorrhage purpuric [MedDRA:10037549]
Hemolytic type rash [MedDRA:10037549]
Purpuric rashes [OMIM:Purpuric rashes]
Mucosa purpura [Orphanet:23610]
Purpura (morphologic abnormality) [Orphanet:23610]
Mucosa petechia [Orphanet:23610]
Purpuras (excl thrombocytopenic) [MedDRA:10037550]
Quality:
Cross references:
Orphanet:23610 "Purpura/petichiae" [Orphanet:23610]
OMIM: "Purpura" [OMIM:Purpura]
OMIM: "Purpuric rashes" [OMIM:Purpuric rashes]
UMLS:C0034150 "Purpura" [HPO:0000979]
UMLS:C0034150 "Purpura" [Orphanet:23610]
Is a (Direct Parents):
HPO         Subcutaneous hemorrhage
Orphanet Vascular skin abnormality
MedDRA Purpura and related conditions
MedDRA Coagulopathies and bleeding diatheses (excl thrombocytopenic)
Orphanet Petechiae
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)
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)