All terms in DOID

Label Id Description
colorectal cancer DOID_9256 [A large intestine cancer that is located_in the colon and/or located_in the rectum.]
obsolete Iris and ciliary body vascular disorder DOID_11525
obsolete Hyphema of iris and ciliary body DOID_11524
obsolete adhesions of drum head to stapes DOID_12854
obsolete Clostridium perfringens gastroenteritis DOID_11523 [A commensal Clostridium infectious disease that is caused by ingestion of food contaminated with Clostridium perfringens, which produces an enterotoxin that acts on the small intestine. The symptoms include watery diarrhea, abdominal cramps, a severe decrease in blood pressure and abdominal expansion from gas.]
obsolete adhesions of drum head to promontorium DOID_12853
obsolete adhesions of drum head to incus DOID_12852
benign hypertensive renal disease DOID_11520
malignant epithelioid hemangioendothelioma DOID_0080190 [A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma.]
choreatic disease DOID_12859 [A movement disease characterized by brief, semi-directed, irregular movements that not repetitive or rhythmic, but appear to flow from one muscle to the next.]
laryngostenosis DOID_11527
Huntington's disease DOID_12858 [A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.]
retrocalcaneal bursitis DOID_12857 [A bursitis that is characterized by an inflammation of the bursa, a fluid-filled sac that cushions the Achilles tendon where it attaches to the heel bone (calcaneus).]
bursitis DOID_2965 [A connective tissue disease that is characterized by the inflammation of bursae, small, fluid-filled sacs that cushion the bones, tendons and muscles near your joints.]
Marinesco-Sjogren syndrome DOID_0080195 [A syndrome characterized by congenital cataracts, cerebellar ataxia, progressive muscle weakness due to myopathy, and delayed psychomotor development.]
mandibulofacial dysostosis, Guion-Almeida type DOID_0080196 [A syndrome characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia.]
congenital muscular dystrophy with cataracts and intellectual disability DOID_0080197 [A congenital muscular dystrophy characterized by onset of progressive muscle weakness in early childhood with autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the INPP5K gene (607875) on chromosome 17p13.]
congenital muscular dystrophy DOID_0050557 [A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.]
infantile histiocytoid cardiomyopathy DOID_0080198 [An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b.]
obsolete PTEN hamartoma tumor syndrome DOID_0080191 [A syndrome comprised of a spectrum of related disorders characterized by the formation of hamartomas, overgrowth, and predisposition to cancer that has_material_basis_in heterozygous germline mutation in the PTEN gene on chromosome 10q23.]