All terms in DOID

Label Id Description
childhood vagina botryoid rhabdomyosarcoma DOID_6787 [A vagina botryoid rhabdomyosarcoma that presents in childhood.]
laryngeal neuroendocrine tumor DOID_5457
patches of hair loss with a black dot pattern SYMP_0020030 [A hair symptom that is characterized by patchy hair loss and the presence of comedo-like cadaver hairs, which appear as black dots.]
Noonan syndrome with multiple lentigines 3 DOID_0080550 [A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the BRAF gene on chromosome 7q34.]
conjunctival congestion SYMP_0020035 [An eye symptom that is characterized by (need def conjunctival congestion - placeholder for xref).]
conjunctival degeneration SYMP_0020036
paroxysmal cough SYMP_0020033 [A cough that is characterized by a persistent cough with sudden onset due to difficulty expelling thick mucus from the tracheobronchial tree. This type of cough is associated with diseases such as Pertussis (Whooping Cough).]
anaplastic thyroid carcinoma DOID_0080522 [A thyroid gland carcinoma that is composed of undifferentiated cells.]
susceptibility to leprosy 5 MIM_613223
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia DOID_0080523 [A leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has_material_basis_in heterozygous mutation in the CSF1R gene on chromosome 5q32.]
thyroid gland adenocarcinoma DOID_0080524 [A thyroid gland carcinoma that derives_from epithelial cells of glandular origin.]
differentiated high-grade thyroid carcinoma DOID_0080525 [A thyroid gland adenocarcinoma characterized by extensive evidence of follicular cell differentiation.]
Tn polyagglutination syndrome DOID_0080520 [A hematopoietic system disease that is characterized by red blood cells that agglutinate upon exposure to almost all human sera, but not to autologous serum or the sera of newborns and has_material_basis_in somatic mutation in the C1GALT1C1 gene on chromosome Xq24.]
lung non-squamous non-small cell carcinoma DOID_0080521 [A lung non-small cell carcinoma that is characterized by the lack of evidence of squamous differentiation.]
bronchiectasis 1 DOID_0080526 [A bronchiectasis that has_material_basis_in mutation in the gene encoding the beta subunit of the epithelial sodium channel on chromosome 16p12.]
bronchiectasis DOID_9563 [A bronchial disease that is a chronic inflammatory condition of one or more bronchi or bronchioles marked by dilatation and loss of elasticity of the walls resulting from damage to the airway wall leading to the formation of small sacs on the bronchial wall and impairment of cilia mobility in the lung. Inflammation of the bronchial wall increases mucus secretion which serves as a breeding ground for bacteria. Bronchiectasis is caused by repeated respiratory infections, immune deficiency disorders, hereditary disorders (cystic fibrosis or primary ciliary dyskinesia), mechanical factors (inhaled object or a lung tumor) or inhaling toxic substances.]
bronchiectasis 2 DOID_0080527 [A bronchiectasis that has_material_basis_in mutation in the gene encoding the alpha subunit of the epithelial sodium channel.]
bronchiectasis 3 DOID_0080528 [A bronchiectasis that has_material_basis_in mutation in the gene encoding the gamma subunit of the epithelial sodium channel.]
Actinomycetaceae NCBITaxon_2049
Actinomycetales NCBITaxon_2037