MedGen

Abnormally increased frequency (usually defined as three or more) loose or watery bowel movements a day. [from HPO]

Gastrointestinal symptoms characterized by chronic abdominal pain and altered bowel habits in the absence of any organic cause. [from NCI]

A clinically heterogeneous spectrum of rare post-infectious neuropathies that usually occur in otherwise healthy patients and encompasses acute inflammatory demyelinating polyradiculoneuropathy (AIDP), acute motor axonal neuropathy (AMAN) and acute motor-sensory axonal neuropathy (AMSAN), Miller-Fisher syndrome (MFS) and some other regional variants. [from ORDO]

The condition of having at least three loose or liquid bowel movements each day. [from MONDO]

Inflammation, or an inflammatory state in the large intestine. [from HPO]

A proneness to anger, i.e., a tendency to become easily bothered or annoyed. [from HPO]

Inflammatory bowel disease is a systemic disorder comprised of two major disorders: ulcerative colitis and Crohn disease. Crohn disease can affect any part of the digestive system while ulcerative colitis is confined to the colon. Both disorders may affect sites outside of the digestive system [from SNOMEDCT_US]

A rare spondyloarthritis characterized by acute or chronic sterile synovitis with or without extra-articular manifestations, becoming manifest after an infection. [from ORDO]

Infections with bacteria of the genus campylobacter. [from MONDO]

Diarrhea-7 (DIAR7) is a protein-losing enteropathy characterized by early-onset nonbloody watery diarrhea and unresponsiveness to soy-based or elemental formulas. Patients experience failure to thrive, hypogammaglobulinemia with recurrent infections, and require albumin infusions and parenteral nutrition. Hypertriglyceridemia and digital clubbing have been observed (Stephen et al., 2016). The malabsorption can result in severe deficiency of vitamin D and other nutrients (Gupta et al., 2020). For a discussion of genetic heterogeneity of diarrhea, see DIAR1 (214700). [from OMIM]

An inflammatory bowel disease that has material basis in variation in the chromosome region 1p36. [from MONDO]

An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1. [from MONDO]