Inflammation of the large intestine
Symptom Information:
Symptom ID: | HPO:0002037 | |||||||||||
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) 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) |
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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) |