Recurrent infection of the gastrointestinal tract
Symptom Information:
Symptom ID: | HPO:0004798 | |||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Recurrent infection of the gastrointestinal tract(HPO:0004798) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Recurrent infections(HPO:0002719) Recurrent infection of the gastrointestinal tract(HPO:0004798) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Recurrent infection of the gastrointestinal tract(HPO:0004798) |
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Database Frequency: | 9 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
COG4-CDG | (Orphanet:263501) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
Hyper-IgM syndrome type 2 | (Orphanet:101089) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
IMMUNOGLOBULIN A DEFICIENCY 1 | (OMIM:137100) |
IMMUNOGLOBULIN A DEFICIENCY 2 | (OMIM:609529) |
Nijmegen breakage syndrome | (Orphanet:647) |
X-linked reticulate pigmentary disorder with systemic manifestations | (Orphanet:85453) |