Pyoderma

Symptom Information:

Symptom ID: HPO:0000999
Synonyms:
Pyoderma [OMIM:Pyoderma]
Pyoderma [MedDRA:10037632]
Quality:
Cross references:
OMIM: "Pyoderma" [OMIM:Pyoderma]
UMLS:C0034212 "Pyoderma" [HPO:0000999]
Is a (Direct Parents):
MedDRA Skin and subcutaneous tissue bacterial infections
HPO         Recurrent bacterial skin 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)
                      Recurrent skin infections(HPO:0001581)
                         Recurrent bacterial skin infections(HPO:0005406)
                            Pyoderma(HPO:0000999)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent bacterial infections(HPO:0002718)
                   Recurrent bacterial skin infections(HPO:0005406)
                      Pyoderma(HPO:0000999)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue infections and infestations(MedDRA:10040792)
       Skin and subcutaneous tissue bacterial infections(MedDRA:10040788)
          Pyoderma(HPO:0000999)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY (OMIM:174770)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST (OMIM:146840)
INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE (OMIM:613148)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Thymic aplasia (Orphanet:83471)