MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandintestinal disease (MONDO:0005020)
..Starting node
..expandsteatorrhea (disease) ()

       Child Nodes:



 Sister Nodes: 
..expandAeromonas hydrophila intestinal disease ()
..expandangiodysplasia of intestine ()
..expandaplasia cutis congenita-intestinal lymphangiectasia syndrome ()
..expandbowel dysfunction ()
..expandchronic atrial and intestinal dysrhythmia ()
..expandchronic enteropathy associated with SLCO2A1 gene ()
..expandchronic intestinal failure ()
..expandchronic intestinal vascular insufficiency ()
..expandcongenital enteropathy involving intestinal mucosa development ()
..expandcongenital intestinal disease due to an enzymatic defect ()
..expandcongenital intestinal transport defect ()
..expandcryptogenic multifocal ulcerous stenosing enteritis ()
..expandcytosolic phospholipase-A2 alpha deficiency associated bleeding disorder ()
..expanddiverticulitis ()
..expandendometriosis of intestine ()
..expandeosinophilic gastrointestinal disease ()
..expandgastroenteritis ()
..expandhypertrophic pyloric stenosis ()
..expandinflammatory bowel disease ()
..expandinguinal hernia ()
..expandintestinal atresia (disease) ()
..expandintestinal lymphangiectasia (disease) ()
..expandintestinal motility disease ()
..expandintestinal neoplasm ()
..expandintestinal obstruction ()
..expandintestinal perforation ()
..expandintractable diarrhea of infancy ()
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..expandlarge intestine disease ()
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..expandmetabolic disease with intestinal involvement ()
..expandmucocele of appendix ()
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..expandneurogenic bowel ()
..expandNK-cell enteropathy ()
..expandparasitic intestinal disease ()
..expandpneumatosis cystoides intestinalis ()
..expandpostgastrectomy syndrome ()
..expandprotein-losing enteropathy (disease) ()
..expandPrP systemic amyloidosis ()
..expandrefractory celiac disease ()
..expandSatoyoshi syndrome ()
..expandshort bowel syndrome ()
..expandsmall intestine disease ()
..expandsolitary rectal ulcer syndrome ()
..expandsteatorrhea (disease) ()
..expandumbilical hernia ()
..expandWhipple disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1075
Name:steatorrhea (disease)
Definition:A finding of an excessive amount of fat in the stool.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:fatty stool; fatty stool (finding); steatorrhea
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: ITCH;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal