Chronic diarrhea

Symptom Information:

Symptom ID: HPO:0002028
Synonyms:
DIARRHEA, RECURRENT [HPO:0002028]
RECURRENT DIARRHEA [HPO:0002028]
Chronic diarrhea (disorder) [Orphanet:27360]
Chronic diarrhea [Orphanet:27360]
Chronic diarrhea [OMIM:Chronic diarrhea]
Diarrhea, recurrent [OMIM:Diarrhea, recurrent]
Malabsorption/chronic diarrhea/steatorrhea [Orphanet:27360]
Chronic diarrhoea [Orphanet:27360]
Diarrhoea [MedDRA:10012735]
Acute diarrhea [MedDRA:10012735]
Antibiotic-associated diarrhea [MedDRA:10012735]
Diarrhea [MedDRA:10012735]
Diarrhea aggravated [MedDRA:10012735]
Diarrhea NOS [MedDRA:10012735]
Diarrhoea aggravated [MedDRA:10012735]
Diarrhoea functional (due to spastic colon) [MedDRA:10012735]
Diarrhoea NOS [MedDRA:10012735]
Explosive diarrhoea [MedDRA:10012735]
Frank diarrhoea [MedDRA:10012735]
Functional diarrhea [MedDRA:10012735]
Functional diarrhoea [MedDRA:10012735]
Functional diarrhoea (due to spastic colon) [MedDRA:10012735]
Iatrogenic diarrhea [MedDRA:10012735]
Iatrogenic diarrhoea [MedDRA:10012735]
Idiopathic diarrhea [MedDRA:10012735]
Loose bowel [MedDRA:10012735]
Loose bowels [MedDRA:10012735]
Loose motions [MedDRA:10012735]
Loose stools [MedDRA:10012735]
Mushy stool [MedDRA:10012735]
Nocturnal diarrhea [MedDRA:10012735]
Secretory diarrhea [MedDRA:10012735]
Stools loose [MedDRA:10012735]
Stools watery [MedDRA:10012735]
Urgent diarrhoea [MedDRA:10012735]
Watery diarrhoea [MedDRA:10012735]
Soft stools [MedDRA:10012735]
Diarrhea functional (due to spastic colon) [MedDRA:10012735]
Explosive diarrhea [MedDRA:10012735]
Frank diarrhea [MedDRA:10012735]
Functional diarrhea (due to spastic colon) [MedDRA:10012735]
Urgent diarrhea [MedDRA:10012735]
Watery diarrhea [MedDRA:10012735]
Acute diarrhoea [MedDRA:10012735]
Antibiotic-associated diarrhoea [MedDRA:10012735]
Idiopathic diarrhoea [MedDRA:10012735]
Nocturnal diarrhoea [MedDRA:10012735]
Secretory diarrhoea [MedDRA:10012735]
Mucous diarrhoea [MedDRA:10012735]
Mucous diarrhea [MedDRA:10012735]
Diarrhoea post chemotherapy [MedDRA:10012735]
Diarrhoea post irradiation [MedDRA:10012735]
Diarrhea post chemotherapy [MedDRA:10012735]
Diarrhea post irradiation [MedDRA:10012735]
Osmotic diarrhea [MedDRA:10012735]
Diarrhea recurrent [MedDRA:10012735]
Diarrhoea recurrent [MedDRA:10012735]
Chronic diarrhea [MedDRA:10012735]
Chronic diarrhoea [MedDRA:10012735]
Mushy diarrhoea [MedDRA:10012735]
Mushy diarrhea [MedDRA:10012735]
Paradoxical diarrhea [MedDRA:10012735]
Paradoxical diarrhoea [MedDRA:10012735]
Malodorous diarrhea [MedDRA:10012735]
Malodourous diarrhoea [MedDRA:10012735]
Osmotic diarrhoea [MedDRA:10012735]
Chronic diarrhea (in some patients) [OMIM:Chronic diarrhea (in some patients)]
Chronic diarrhea (seen in recessive form) [OMIM:Chronic diarrhea (seen in recessive form)]
Diarrhea (HCP) [OMIM:Diarrhea (HCP)]
Diarrhea (due to vasoactive intestinal peptide) [OMIM:Diarrhea (due to vasoactive intestinal peptide)]
Diarrhea (in 1 patient) [OMIM:Diarrhea (in 1 patient)]
Diarrhea (in severe cases) [OMIM:Diarrhea (in severe cases)]
Diarrhea (in some patients) [OMIM:Diarrhea (in some patients)]
Diarrhea, chronic [OMIM:Diarrhea, chronic]
Diarrhea, recurrent (1 patient) [OMIM:Diarrhea, recurrent (1 patient)]
Diarrhea, recurrent (less common) [OMIM:Diarrhea, recurrent (less common)]
Diarrhea, secretory [OMIM:Diarrhea, secretory]
Diarrhea, watery [OMIM:Diarrhea, watery]
Recurrent diarrhea (1 patient) [OMIM:Recurrent diarrhea (1 patient)]
Watery diarrhea (children and adults) [OMIM:Watery diarrhea (children and adults)]
Diarrhoea (excl infective) [MedDRA:10012736]
Quality:
Cross references:
Orphanet:27360 "Malabsorption/chronic diarrhea/steatorrhea" [Orphanet:27360]
OMIM: "Chronic diarrhea" [OMIM:Chronic diarrhea]
OMIM: "Diarrhea, recurrent" [OMIM:Diarrhea, recurrent]
OMIM: "Chronic diarrhea (in some patients)" [OMIM:Chronic diarrhea (in some patients)]
OMIM: "Chronic diarrhea (seen in recessive form)" [OMIM:Chronic diarrhea (seen in recessive form)]
OMIM: "Diarrhea (HCP)" [OMIM:Diarrhea (HCP)]
OMIM: "Diarrhea (due to vasoactive intestinal peptide)" [OMIM:Diarrhea (due to vasoactive intestinal peptide)]
OMIM: "Diarrhea (in 1 patient)" [OMIM:Diarrhea (in 1 patient)]
OMIM: "Diarrhea (in severe cases)" [OMIM:Diarrhea (in severe cases)]
OMIM: "Diarrhea (in some patients)" [OMIM:Diarrhea (in some patients)]
OMIM: "Diarrhea, chronic" [OMIM:Diarrhea, chronic]
OMIM: "Diarrhea, recurrent (1 patient)" [OMIM:Diarrhea, recurrent (1 patient)]
OMIM: "Diarrhea, recurrent (less common)" [OMIM:Diarrhea, recurrent (less common)]
OMIM: "Diarrhea, secretory" [OMIM:Diarrhea, secretory]
OMIM: "Diarrhea, watery" [OMIM:Diarrhea, watery]
OMIM: "Recurrent diarrhea (1 patient)" [OMIM:Recurrent diarrhea (1 patient)]
OMIM: "Watery diarrhea (children and adults)" [OMIM:Watery diarrhea (children and adults)]
UMLS:C0401151 "Chronic diarrhea" [Orphanet:27360]
Is a (Direct Parents):
MedDRA Gastrointestinal motility and defaecation conditions
MedDRA Diarrhea
Orphanet Malabsorption
Orphanet Functional anomalies of the digestive system
HPO         Diarrhea
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)
       Diarrhea(HPO:0002014)
          Chronic diarrhea(HPO:0002028)
       Chronic diarrhea(HPO:0002028)
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)