Diarrhea
Symptom Information:
Symptom ID: | HPO:0002014 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal motility and defaecation conditions(MedDRA:10017977) Diarrhea(HPO:0002014) |
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Database Frequency: | 225 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
5-oxoprolinase deficiency | (Orphanet:33572) |
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE | (OMIM:601495) |
AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE | (OMIM:613501) |
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE | (OMIM:613502) |
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE | (OMIM:612692) |
AGAMMAGLOBULINEMIA, X-LINKED | (OMIM:300755) |
AL amyloidosis | (Orphanet:85443) |
ALG3-CDG | (Orphanet:79321) |
ATTRV122I amyloidosis | (Orphanet:85451) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Acute intermittent porphyria | (Orphanet:79276) |
Adiposis dolorosa | (Orphanet:36397) |
Adult intestinal botulism | (Orphanet:178487) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Aspartylglucosaminuria | (Orphanet:93) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Autoimmune lymphoproliferative syndrome with recurrent infections | (Orphanet:275517) |
Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Barth syndrome | (Orphanet:111) |
Bartter syndrome | (Orphanet:112) |
Biotinidase deficiency | (Orphanet:79241) |
Bloom syndrome | (Orphanet:125) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Botulism | (Orphanet:1267) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
COG4-CDG | (Orphanet:263501) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Carney triad | (Orphanet:139411) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Central diabetes insipidus | (Orphanet:178029) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Cholera | (Orphanet:173) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Chronic diarrhea due to guanylate cyclase 2C overactivity | (Orphanet:314373) |
Chylomicron retention disease | (Orphanet:71) |
Classic galactosemia | (Orphanet:79239) |
Cogan syndrome | (Orphanet:1467) |
Cold agglutinin disease | (Orphanet:56425) |
Combined immunodeficiency due to ZAP70 deficiency | (Orphanet:911) |
Combined malonic and methylmalonic acidemia | (Orphanet:289504) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Congenital chloride diarrhea | (Orphanet:53689) |
Congenital enteropathy due to enteropeptidase deficiency | (Orphanet:168601) |
Congenital lactase deficiency | (Orphanet:53690) |
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells | (Orphanet:83620) |
Congenital sucrase-isomaltase deficiency | (Orphanet:35122) |
Congenital toxoplasmosis | (Orphanet:858) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cutaneous photosensitivity - lethal colitis | (Orphanet:2881) |
Cyclic neutropenia | (Orphanet:2686) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
DIARRHEA 7 | (OMIM:615863) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
Dengue fever | (Orphanet:99828) |
Desminopathy | (Orphanet:98909) |
Diarrhea-vomiting due to trehalase deficiency | (Orphanet:103909) |
Distomatosis | (Orphanet:1685) |
Dracunculiasis | (Orphanet:231) |
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
ENTEROPATHY, PROTEIN-LOSING | (OMIM:226300) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Familial dysautonomia | (Orphanet:1764) |
Familial visceral myopathy | (Orphanet:2604) |
Fanconi syndrome - ichthyosis - dysmorphism | (Orphanet:1981) |
Foodborne botulism | (Orphanet:228371) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE III | (OMIM:613960) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized juvenile polyposis/juvenile polyposis coli | (Orphanet:329971) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Glutaric acidemia type 3 | (Orphanet:35706) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency | (Orphanet:79240) |
Glycogen storage disease due to phosphorylase kinase deficiency | (Orphanet:370) |
Good syndrome | (Orphanet:169105) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION | (OMIM:601979) |
Hawkinsinuria | (Orphanet:2118) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hereditary angioedema type 1 | (Orphanet:100050) |
Hereditary angioedema type 2 | (Orphanet:100051) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hirschsprung disease | (Orphanet:388) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Hypouricemia, renal, 2 | (OMIM:612076) |
ICF syndrome | (Orphanet:2268) |
IMMUNODEFICIENCY 19 | (OMIM:615617) |
IMMUNODEFICIENCY 22 | (OMIM:615758) |
IMMUNODEFICIENCY 31C | (OMIM:614162) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 | (OMIM:242860) |
INFLAMMATORY BOWEL DISEASE 1 | (OMIM:266600) |
INFLAMMATORY BOWEL DISEASE 11 | (OMIM:191390) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Inhalational botulism | (Orphanet:254504) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Intestinal botulism | (Orphanet:178481) |
Isolated agammaglobulinemia | (Orphanet:229717) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Kawasaki disease | (Orphanet:2331) |
LACTOSE INTOLERANCE, ADULT TYPE | (OMIM:223100) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
Lassa fever | (Orphanet:99824) |
Legionellosis | (Orphanet:549) |
Lujo hemorrhagic fever | (Orphanet:319213) |
Lysinuric protein intolerance | (Orphanet:470) |
Lysosomal acid lipase deficiency | (Orphanet:275761) |
MEDNIK syndrome | (Orphanet:171851) |
MELAS | (Orphanet:550) |
METHIONINE MALABSORPTION SYNDROME | (OMIM:250900) |
MITCHELL-RILEY SYNDROME | (OMIM:615710) |
MPI-CDG | (Orphanet:79319) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
Malakoplakia | (Orphanet:556) |
Malonic aciduria | (Orphanet:943) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Mastocytosis | (Orphanet:98292) |
Mevalonic aciduria | (Orphanet:29) |
Microscopic polyangiitis | (Orphanet:727) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII | (OMIM:615548) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal inflammatory skin and bowel disease | (Orphanet:294023) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Neuroblastoma | (Orphanet:635) |
Nijmegen breakage syndrome | (Orphanet:647) |
Non-histaminic angioedema | (Orphanet:658) |
Obesity due to prohormone convertase I deficiency | (Orphanet:71528) |
Omenn syndrome | (Orphanet:39041) |
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | (OMIM:615399) |
PMM2-CDG | (Orphanet:79318) |
Paroxysmal cold hemoglobinuria | (Orphanet:90035) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Porphyria | (Orphanet:738) |
Primary erythermalgia | (Orphanet:90026) |
Primary systemic amyloidosis | (Orphanet:314701) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Progressive familial intrahepatic cholestasis type 1 | (Orphanet:79306) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
Progressive familial intrahepatic cholestasis type 3 | (Orphanet:79305) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
RAPADILINO syndrome | (Orphanet:3021) |
Rabies | (Orphanet:770) |
Recurrent infections associated with rare immunoglobulin isotypes deficiency | (Orphanet:183675) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |
Reticular dysgenesis | (Orphanet:33355) |
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications | (Orphanet:3018) |
Rift valley fever | (Orphanet:319251) |
SATOYOSHI SYNDROME | (OMIM:600705) |
Sanfilippo syndrome type A | (Orphanet:79269) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Sanfilippo syndrome type C | (Orphanet:79271) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Scheie syndrome | (Orphanet:93474) |
Senile systemic amyloidosis | (Orphanet:330001) |
Severe combined immunodeficiency due to DCLRE1C deficiency | (Orphanet:275) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Severe combined immunodeficiency due to complete RAG1/2 deficiency | (Orphanet:331206) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | (Orphanet:632) |
Sodium channelopathy-related small fiber neuropathy | (Orphanet:306577) |
Spontaneous periodic hypothermia | (Orphanet:29822) |
Syndromic diarrhea | (Orphanet:84064) |
Syndromic multisystem autoimmune disease due to Itch deficiency | (Orphanet:228426) |
Systemic capillary leak syndrome | (Orphanet:188) |
T-B+ severe combined immunodeficiency due to CD45 deficiency | (Orphanet:169157) |
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency | (Orphanet:169154) |
T-B+ severe combined immunodeficiency due to JAK3 deficiency | (Orphanet:35078) |
TRAPS syndrome | (Orphanet:32960) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |
Transcobalamin deficiency | (Orphanet:859) |
Transketolase deficiency | (ORPHA:488618) |
Typhoid | (Orphanet:99745) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Viral hemorrhagic fever | (Orphanet:341) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolman disease | (Orphanet:75233) |
X-linked agammaglobulinemia | (Orphanet:47) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
Yellow fever | (Orphanet:99829) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |