Perianal abscess

Symptom Information:

Symptom ID: HPO:0009789
Synonyms:
Perianal abscess [OMIM:Perianal abscess]
Perianal abscess (rare) [OMIM:Perianal abscess (rare)]
Quality:
Cross references:
OMIM: "Perianal abscess" [OMIM:Perianal abscess]
OMIM: "Perianal abscess (rare)" [OMIM:Perianal abscess (rare)]
Is a (Direct Parents):
HPO         Recurrent cutaneous abscess formation
HPO         Abnormality of the anus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the anus(HPO:0004378)
                   Perianal abscess(HPO:0009789)
       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)
                            Recurrent cutaneous abscess formation(HPO:0100838)
                               Perianal abscess(HPO:0009789)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent abscess formation(HPO:0002722)
                   Recurrent cutaneous abscess formation(HPO:0100838)
                      Perianal abscess(HPO:0009789)
                Recurrent bacterial infections(HPO:0002718)
                   Recurrent bacterial skin infections(HPO:0005406)
                      Recurrent cutaneous abscess formation(HPO:0100838)
                         Perianal abscess(HPO:0009789)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive early-onset inflammatory bowel disease (Orphanet:238569)
Currarino triad (Orphanet:1552)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE (OMIM:613148)