All terms in DOID

Label Id Description
susceptibility to partial acquired lipodystrophy MIM_608709
obsolete syndrome of infant of a diabetic mother DOID_14045
Her2-receptor positive breast cancer DOID_0060079 [A breast cancer that is characterized by the presence of Her2 receptors.]
progesterone-receptor negative breast cancer DOID_0060078 [A breast cancer that is characterized by the absence of progesterone receptors.]
progesterone-receptor positive breast cancer DOID_0060077 [A breast cancer that is characterized by the presence of progesterone receptors.]
estrogen-receptor negative breast cancer DOID_0060076 [A breast cancer that is characterized by the absence of estrogen receptors.]
estrogen-receptor positive breast cancer DOID_0060075 [A breast cancer that is characterized by the presence of estrogen receptors.]
immune system cancer DOID_0060083 [An organ system cancer located_in the immune system that is characterized by uncontrolled cellular proliferation in organs of the immune system.]
obsolete Bacillus cereus pneumonia DOID_0060069
obsolete rheumatic endocarditis DOID_14056
Sauropsida NCBITaxon_8457
Pearson syndrome DOID_0060067 [A mitochondrial metabolism disease that is characterized by sideroblastic anemia and exocrine pancreas dysfunction.]
pyridoxine-responsive sideroblastic anemia DOID_0060066 [A sideoblastic anemia that is characterized by the presence of microcytic hypochromic anemia and iron overload, and has_material_basis_in X-linked inheritance.]
autosomal recessive pyridoxine-refractory sideroblastic anemia 2 DOID_0060065 [A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and has_material_basis_in autosomal recessive inheritance of mutation in the SLC25A38 gene.]
obsolete sideroblastic anemia with spinocerebellar ataxia DOID_0060064 [A sideoblastic anemia that is characterized by microcytic hypochromic anemia and ealy-onset, slowly progressive spinocerebellar ataxia, and has_material_basis_in X-linked inheritance of mutation in the ABCB7 gene that encodes a transporter protein that plays a role in heme production in the bone marrow and cerebellum.]
sideroblastic anemia 1 DOID_0060063 [A sideoblastic anemia that is characterized by the presence of microcytic hypochromic anemia and iron overload, and has_material_basis_in X-linked inheritance of mutation in the ALAS2 gene that enocdes aminolevulinic acid synthase that catalyzes the first step in heme production.]
Abnormal circulating lipid concentration HP_0003119
obsolete acute glomerulonephritis with lesion of rapidly progressive glomerulonephritis DOID_14063
acute poststreptococcal glomerulonephritis DOID_14064
acute diffuse nephritis DOID_14066