Pustule

Symptom Information:

Symptom ID: HPO:0200039
Synonyms:
Pustula [HPO:0200039]
Skin pustule [HPO:0200039]
Skin pustule [Orphanet:23340]
Pustule (morphologic abnormality) [Orphanet:23340]
Pustule (disorder) [Orphanet:23340]
pustule [HPO:0200039]
pustule [Orphanet:23340]
Pustula/pustulosis [Orphanet:23340]
Pustule [Orphanet:23340]
Rash pustular [MedDRA:10037888]
Pustular rash [MedDRA:10037888]
Pustular skin eruption [MedDRA:10037888]
Pustule [MedDRA:10037888]
Pustules on hand [MedDRA:10037888]
Rash vesiculo-pustular [MedDRA:10037888]
Rash vesiculopustular [MedDRA:10037888]
Vesiculo-pustular rash [MedDRA:10037888]
Vesiculopustular rash [MedDRA:10037888]
Papulopustular rash [MedDRA:10037888]
Pustular rash [OMIM:Pustular rash]
Quality:
Cross references:
Orphanet:23340 "Pustula/pustulosis" [Orphanet:23340]
OMIM: "Pustular rash" [OMIM:Pustular rash]
UMLS:C0241157 "pustule" [HPO:0200039]
UMLS:C0241157 "pustule" [Orphanet:23340]
Is a (Direct Parents):
Orphanet Abnormality of the skin
HPO         Inflammatory abnormality of the skin
MedDRA Skin structures and soft tissue infections
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)
                Abnormality of skin physiology(HPO:0011122)
                   Inflammatory abnormality of the skin(HPO:0011123)
                      Pustule(HPO:0200039)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Skin structures and soft tissue infections(MedDRA:10040786)
          Pustule(HPO:0200039)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Bullous impetigo (Orphanet:36237)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Epidermodysplasia verruciformis (Orphanet:302)
Erosive pustular dermatosis of the scalp (Orphanet:222)
Generalized pustular psoriasis (Orphanet:247353)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2 (OMIM:616069)
Immunoglobulin A vasculitis (Orphanet:761)
Lipoid proteinosis (Orphanet:530)
Majeed syndrome (Orphanet:77297)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Papillon-Lefèvre syndrome (Orphanet:678)
Pityriasis rubra pilaris (Orphanet:2897)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Quinquaud's folliculitis decalvans (Orphanet:346)
Reactive arthritis (Orphanet:29207)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Subcorneal pustular dermatosis (Orphanet:48377)
Sweet syndrome (Orphanet:3243)