Chronic diarrhea
Symptom Information:
Symptom ID: | HPO:0002028 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Abdominal symptom(HPO:0011458) Diarrhea(HPO:0002014) Chronic diarrhea(HPO:0002028) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal motility and defaecation conditions(MedDRA:10017977) Chronic diarrhea(HPO:0002028) Diarrhea(HPO:0002014) Chronic diarrhea(HPO:0002028) |
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Database Frequency: | 51 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autoimmune lymphoproliferative syndrome with recurrent infections | (Orphanet:275517) |
BILE ACID MALABSORPTION, PRIMARY | (OMIM:613291) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
COG4-CDG | (Orphanet:263501) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
CONGENITAL SHORT BOWEL SYNDROME | (OMIM:615237) |
Congenital chloride diarrhea | (Orphanet:53689) |
Congenital sucrase-isomaltase deficiency | (Orphanet:35122) |
Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
Cystinosis | (Orphanet:213) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
Dubowitz syndrome | (Orphanet:235) |
Ethylmalonic encephalopathy | (Orphanet:51188) |
GOLGI REASSEMBLY STACKING PROTEIN 1 | (OMIM:606867) |
Glucose-galactose malabsorption | (Orphanet:35710) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
IMMUNODEFICIENCY 15 | (OMIM:615592) |
IMMUNODEFICIENCY, COMMON VARIABLE, 11 | (OMIM:615767) |
IMMUNODEFICIENCY, COMMON VARIABLE, 7 | (OMIM:614699) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
MELAS | (Orphanet:550) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Menkes disease | (Orphanet:565) |
Mulibrey nanism | (Orphanet:2576) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
Occipital horn syndrome | (Orphanet:198) |
Pearson syndrome | (Orphanet:699) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
Recurrent infections associated with rare immunoglobulin isotypes deficiency | (Orphanet:183675) |
SENER SYNDROME | (OMIM:606156) |
Sandhoff disease | (Orphanet:796) |
Sandhoff disease, adult form | (Orphanet:309169) |
Sandhoff disease, infantile form | (Orphanet:309155) |
Sandhoff disease, juvenile form | (Orphanet:309162) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Syndromic multisystem autoimmune disease due to Itch deficiency | (Orphanet:228426) |
T-B+ severe combined immunodeficiency due to gamma chain deficiency | (Orphanet:276) |
Thymic aplasia | (Orphanet:83471) |
Wolfram syndrome | (Orphanet:3463) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |