WormMine: DiseaseOntology DOID:0080682 autosomal dominant familial visceral neuropathy Disease Ontology

Name
Disease Ontology

Identifier	Name	Description
DOID:7	disease of anatomical entity	A disease that manifests in a defined anatomical structure.
DOID:4	disease	A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:77	gastrointestinal system disease	A disease of anatomical entity that is located_in the gastrointestinal tract.
DOID:0050177	monogenic disease	A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630	genetic disease	A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050736	autosomal dominant disease	An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.
DOID:0050739	autosomal genetic disease	A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:5295	intestinal disease	A gastrointestinal system disease that is located_in the intestine.
DOID:5353	colonic disease	A intestinal disease located in the colon.
DOID:0080072	intestinal pseudo-obstruction	A colonic disease that is characterized by bowel obstruction resulting from impairment of the muscle contractions that move food through the digestive tract.
DOID:0080682	autosomal dominant familial visceral neuropathy	An intestinal pseudo-obstruction that is inherited as an autosomal dominant trait.

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