Enterocolitis

Symptom Information:

Symptom ID: HPO:0004387
Synonyms:
Enterocolitis [OMIM:Enterocolitis]
Enterocolitis [MedDRA:10014893]
Quality:
Cross references:
OMIM: "Enterocolitis" [OMIM:Enterocolitis]
UMLS:C0014356 "Enterocolitis" [HPO:0004387]
Is a (Direct Parents):
MedDRA Gastrointestinal inflammatory disorders NEC
HPO         Acute colitis
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)
                Gastrointestinal inflammation(HPO:0004386)
                   Inflammation of the large intestine(HPO:0002037)
                      Colitis(HPO:0002583)
                         Acute colitis(HPO:0100282)
                            Enterocolitis(HPO:0004387)
                Abnormality of the intestine(HPO:0002242)
                   Abnormality of the large intestine(HPO:0002250)
                      Colitis(HPO:0002583)
                         Acute colitis(HPO:0100282)
                            Enterocolitis(HPO:0004387)
                   Inflammation of the large intestine(HPO:0002037)
                      Colitis(HPO:0002583)
                         Acute colitis(HPO:0100282)
                            Enterocolitis(HPO:0004387)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal inflammatory conditions(MedDRA:10017969)
       Gastrointestinal inflammatory disorders NEC(MedDRA:10017921)
          Enterocolitis(HPO:0004387)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

5-oxoprolinase deficiency (Orphanet:33572)
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS (OMIM:616050)
Autosomal recessive early-onset inflammatory bowel disease (Orphanet:238569)
ENTEROCOLITIS (OMIM:226150)
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:142623)
Hirschsprung disease (Orphanet:388)
INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE (OMIM:613148)