All terms in DOID

Label Id Description
B-lymphoblastic leukemia with ZNF384 rearrangement DOID_0070628 [A B-lymphoblastic leukemia/lymphoma associated with ZNF384 gene rearrangement.]
Abnormal eye physiology HP_0012373
Abnormality of the eye HP_0000478
Pisoniviricetes NCBITaxon_2732506
Pisuviricota NCBITaxon_2732408
acute myeloid leukemia with CBFA2T3-GLIS2 fusion DOID_0070629 [An acute myeloid leukemia associated with CBFA2T3-GLIS2 chimeric oncogene.]
Abnormal eye morphology HP_0012372
Human immunodeficiency virus 2 NCBITaxon_11709
B-lymphoblastic leukemia with PAX5alt DOID_0070626 [A B-lymphoblastic leukemia/lymphoma associated with PAX5 gene alteration, including rearrangements, point mutations, and intragenic lesions.]
B-lymphoblastic leukemia with TCF3-HLF fusion DOID_0070627 [A B-lymphoblastic leukemia/lymphoma associated with TCF3-HLF gene rearrangement.]
tetanic convulsion SYMP_0000327 [A convulsion that is characterized by a tonic spasm (prolonged contraction of the muscles), without loss of consciousness and often associated with hypocalcemia.]
mild tetanic convulsion SYMP_0000328 [A tetanic convulsion that is not intense (not severe).]
splice_donor_region_variant SO_0002170
mild bronchitis SYMP_0000325
bronchitis SYMP_0000324 [A respiratory system and chest symptom that is characterized by an acute or chronic inflammation of the bronchial tubes.]
mild hypotension SYMP_0000326
cardiovascular-kidney-metabolic syndrome DOID_0070635 [A syndrome characterized by multiorgan dysfunction and a high rate of adverse cardiovascular outcomes arising from the interconnection between cardiovascular disease, chronic kidney disease, and metabolic risk factors associated with diabetes and obesity.]
mirror movements 1 DOID_0070636 [A congenital mirror movement disorder characterized by mirror movements and/or agenesis of the corpus callosum that has_material_basis_in heterozygous mutation in the DCC gene on chromosome 18q21, with incomplete penetrance.]
congenital mirror movement disorder DOID_0111153 [A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs.]
acute myeloid leukemia with NPM1-MLF1 fusion DOID_0070633 [An acute myeloid leukemia associated with NPM1-MLF1 gene fusion.]