Inflammation of the large intestine

Symptom Information:

Symptom ID: HPO:0002037
Synonyms:
Inflammatory bowel disease [HPO:0002037]
Inflammatory bowel disease [Orphanet:27570]
Inflammatory bowel disease (disorder) [Orphanet:27570]
Inflammatory Bowel Diseases [Orphanet:27570]
Inflammatory bowel disease [OMIM:Inflammatory bowel disease]
Inflammatory intestinal disease [Orphanet:27570]
Inflammatory bowel disease [MedDRA:10021972]
IBD [MedDRA:10021972]
Inflammatory bowel disease NOS [MedDRA:10021972]
Inflammatory bowel disease (1 patient) [OMIM:Inflammatory bowel disease (1 patient)]
Inflammatory bowel disease (Crohns disease and ulcerative colitis) [OMIM:Inflammatory bowel disease (Crohns disease and ulcerative colitis)]
Quality:
Cross references:
Orphanet:27570 "Inflammatory intestinal disease" [Orphanet:27570]
OMIM: "Inflammatory bowel disease" [OMIM:Inflammatory bowel disease]
OMIM: "Inflammatory bowel disease (1 patient)" [OMIM:Inflammatory bowel disease (1 patient)]
OMIM: "Inflammatory bowel disease (Crohns disease and ulcerative colitis)" [OMIM:Inflammatory bowel disease (Crohns disease and ulcerative colitis)]
UMLS:C0021390 "Inflammatory Bowel Diseases" [Orphanet:27570]
Is a (Direct Parents):
HPO         Gastrointestinal inflammation
MedDRA Colitis
HPO         Abnormality of the intestine
Orphanet Functional anomalies of the digestive system
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)
                   Inflammation of the large intestine(HPO:0002037)
                Gastrointestinal inflammation(HPO:0004386)
                   Inflammation of the large intestine(HPO:0002037)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal inflammatory conditions(MedDRA:10017969)
       Colitis(HPO:0002583)
          Inflammation of the large intestine(HPO:0002037)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl (OMIM:614576)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
IMMUNODEFICIENCY, COMMON VARIABLE, 11 (OMIM:615767)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
INFLAMMATORY BOWEL DISEASE 11 (OMIM:191390)
INFLAMMATORY BOWEL DISEASE 13 (OMIM:612244)
INFLAMMATORY BOWEL DISEASE 19 (OMIM:612278)
Kindler syndrome (Orphanet:2908)
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA (OMIM:608809)
Pseudomyxoma peritonei (Orphanet:26790)
Reactive arthritis (Orphanet:29207)
SAPHO syndrome (Orphanet:793)
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:106300)
Sarcoidosis (Orphanet:797)
Secondary intestinal lymphangiectasia (Orphanet:90363)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wiskott-Aldrich syndrome (Orphanet:906)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 (OMIM:612541)