Rectal abscess

Symptom Information:

Symptom ID: HPO:0005224
Synonyms:
Perirectal abscess [HPO:0005224]
Perirectal abscesses [OMIM:Perirectal abscesses]
Rectal abscess [MedDRA:10048947]
Perirectal abscess [MedDRA:10052814]
Quality:
Cross references:
OMIM: "Perirectal abscesses" [OMIM:Perirectal abscesses]
Is a (Direct Parents):
HPO         Abnormality of the rectum
HPO         Recurrent abscess formation
MedDRA Abdominal and gastrointestinal infections
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 intestine(HPO:0002242)
                   Abnormality of the large intestine(HPO:0002250)
                      Abnormality of the rectum(HPO:0002034)
                         Rectal abscess(HPO:0005224)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent abscess formation(HPO:0002722)
                   Rectal abscess(HPO:0005224)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Abdominal and gastrointestinal infections(MedDRA:10017967)
          Rectal abscess(HPO:0005224)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive early-onset inflammatory bowel disease (Orphanet:238569)
Cyclic neutropenia (Orphanet:2686)
Familial caudal dysgenesis (Orphanet:1768)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE (OMIM:233690)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I (OMIM:233700)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II (OMIM:233710)
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED (OMIM:306400)
Leukocyte adhesion deficiency (Orphanet:2968)
Leukocyte adhesion deficiency type I (Orphanet:99842)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)