All terms in DOID

Label Id Description
aflatoxins-related hepatocellular carcinoma DOID_5022
maxillary sinus adenocarcinoma DOID_7684
maxillary sinus cancer DOID_1357
pancreatic non-invasive intraductal papillary-mucinous carcinoma DOID_7685
pancreatic intraductal papillary-colloid carcinoma DOID_7574
chronic lymphocytic leukemia/small lymphocytic lymphoma DOID_6354 [A chronic lymphocytic leukemia that is characterized by the presence of immature lymphocytes in the blood and bone marrow and/or in the lymph nodes.]
obsolete recurrent hepatocellular carcinoma DOID_5027
sclerosing hepatic carcinoma DOID_5026
obsolete Alphavirus infectious disease DOID_5029 [A Togaviridae infectious disease that results_in infection in animals and humans, has_material_basis_in Alphavirus, which is transmitted_by mosquito bite.]
glycogen storage disease Ib DOID_0081330 [A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23.]
glycogen storage disease I DOID_0081329 [A glycogen storage disease that is characterized by severe hypoglycemia and hepatomegaly caused by the accumulation of glycogen. Affected individuals exhibit growth retardation, delayed puberty, lactic acidemia, hyperlipidemia, hyperuricemia, and in adults a high incidence of hepatic adenomas.]
leptomeninges sarcoma DOID_7689
malignant leptomeningeal neoplasm DOID_6086
obsolete recurrent cancer of Liver DOID_5028
glycogen storage disease Ic DOID_0081331 [A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23. G6PT1 is also the site of the defect in glycogen storage disease Ib.]
Weight loss HP_0001824
Decreased body weight HP_0004325
congenital myopathy 15 DOID_0081347 [A congenital myopathy that is characterized by symptom onset soon after birth and that has_material_basis_in heterozygous mutation in the TNNC2 gene on chromosome 20q13. Affected infants are hypotonic and have severe respiratory insufficiency and feeding problems, sometimes requiring mechanical ventilation or tube feeding.]
congenital myopathy 16 DOID_0081348 [A congenital myopathy that is characterized by onset of hypotonia and tremor in infancy and that has_material_basis_in heterozygous mutation in the MYBPC1 gene on chromosome 12q23. Patients have mildly delayed walking, unsteady gait, proximal muscle weakness, and a high-frequency tremor of the limbs.]
obsolete olivopontocerebellar atrophy V DOID_0080017