All terms in DOID

Label Id Description
Klatskin's tumor DOID_4927 [An intrahepatic cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts.]
intrahepatic cholangiocarcinoma DOID_4928 [A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree.]
bronchiolo-alveolar adenocarcinoma DOID_4926 [A lung adenocarcinoma characterized by a predominantly lepidic pattern and 5 mm or less invasion in greatest dimension.]
lung adenocarcinoma DOID_3910 [A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.]
tubular adenocarcinoma DOID_4929 [An adenocarcinoma that derives_from epithelial cells originating in glandular tissue. The tumor has branched angular tubules embedded in a loose fibrous stroma.]
hyaline cartilage tissue UBERON_0001994
cartilage tissue UBERON_0002418
Opisthokonta NCBITaxon_33154
placenta UBERON_0001987
eccrine sweat gland cancer DOID_4921
eccrine adenocarcinoma DOID_4920 [An eccrine sweat gland cancer that derives_from epithelial cells of glandular origin.]
thymus adenocarcinoma DOID_4923 [A thymic carcinoma that derives_from epithelial cells of glandular origin.]
breast secretory carcinoma DOID_4922 [A breast adenocarcinoma that has_material_basis_in cells with abundant granular or clear vacuolated cytoplasm.]
oculopharyngodistal myopathy 3 DOID_0081299 [An oculopharyngodistal myopathy that is characterized by progressive muscle weakness with ocular, facial, pharyngeal, and distal limb involvement, resulting in dysarthria and gait difficulties and that has_material_basis_in heterozygous trinucleotide repeat expansion (CGG) in the 5-prime untranslated region (UTR) of the NOTCH2NLC gene on chromosome 1q21.]
oculopharyngodistal myopathy DOID_0081296 [A myopathy that is characterized by progressive external ocular, facial and pharyngeal muscle weakness, leading to variable degrees of ptosis, ophthalmoparesis, facial muscle atrophy, dysarthria and dysphagia, as well as distal muscle weakness and atrophy of lower and upper extremities.]
Antley-Bixler syndrome without disordered steroidogenesis DOID_0081290 [An Antley-Bixler syndrome that has_material_basis_in heterozygous mutation in a fibroblast growth factor receptor gene, FGFR2, on chromosome 10q26 and is an exclusively skeletal form of Antley-Bixler syndrome.]
Antley-Bixler syndrome DOID_0081289 [A craniosynostosis that is characterized by radiohumeral synostosis present from the perinatal period.]
essential tremor 6 DOID_0081295 [An essential tremor that is characterized by adult-onset kinetic and/or postural tremor usually affecting the upper limbs and that has_material_basis_in heterozygous trinucleotide GGC repeat expansion in the 5-prime untranslated region of the NOTCH2NLC gene on chromosome 1q21.]
myopathy DOID_423 [A muscular disease in which the muscle fibers do not function resulting in muscular weakness.]
oculopharyngodistal myopathy 1 DOID_0081297 [An oculopharyngodistal myopathy that is characterized by adult-onset ptosis, external ophthalmoplegia, facial muscle weakness, distal limb muscle weakness and atrophy, and pharyngeal involvement, resulting in dysphagia and dysarthria, and that has_material_basis_in heterozygous trinucleotide repeat expansion (CGG) in the 5-prime untranslated region of the LRP12 gene on chromosome 8q22.]