All terms in DOID

Label Id Description
childhood supratentorial ependymoma DOID_7502
obsolete Hodgkin's lymphoma, lymphocytic-histiocytic predominance involving lymph nodes of multiple sites DOID_8832
periumbilic pelvic swelling SYMP_0000795
obsolete herpes zoster keratoconjunctivitis DOID_8839 [An ophthalmic herpes zoster that results_in inflammation located_in cornea and located_in conjunctiva, has_material_basis_in Human herpesvirus 3, which reactivates from the trigeminal ganglion after the primary infection and has_symptom red eye, has_symptom irritation, and has_symptom pain.]
obsolete malformation of placenta DOID_7507
epigastric pelvic swelling SYMP_0000792
Hodgkin's lymphoma, nodular sclerosis DOID_8838
Hodgkin's lymphoma DOID_8567 [A lymphoma that is marked by the presence of a type of cell called the Reed-Sternberg cell.]
left lower quadrant pelvic swelling SYMP_0000793
obsolete Hodgkin's lymphoma, nodular sclerosis, involving lymph nodes of head, face, and neck DOID_8837
multiple sites pelvic swelling SYMP_0000790
small intestinal L-cell glucagon-like peptide producing tumor DOID_7506
obsolete Burkitt's tumor or lymphoma involving lymph nodes of head, face, and neck DOID_8836
generalized pelvic swelling SYMP_0000791
developmental and epileptic encephalopathy 61 DOID_0080434 [A developmental and epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the ADAM22 gene on chromosome 7q21.]
developmental and epileptic encephalopathy 37 DOID_0080435 [A developmental and epileptic encephalopathy characterized by onset of intractable seizures or abnormal movement in the first years of life and developmental delay or regression after seizure onset that has_material_basis_in homozygous or compound heterozygous mutation in the FRRS1L gene (604574) on chromosome 9q31.]
developmental and epileptic encephalopathy 4 DOID_0080436 [A developmental and epileptic encephalopathy characterized by onset of tonic seizures in early infancy and severely impaired psychomotor development that has_material_basis_in heterozygous mutation in the STXBP1 gene on chromosome 9q34.1.]
Nairoviridae NCBITaxon_1980415
developmental and epileptic encephalopathy 31A DOID_0080437 [A developmental and epileptic encephalopathy characterized by onset in the first months or years of life of refractory seizures and global developmental delay from early infancy that has_material_basis_in heterozygous mutation in the DNM1 gene on chromosome 9q34.]
developmental and epileptic encephalopathy 65 DOID_0080430 [A developmental and epileptic encephalopathy characterized by onset in the first months to years of life of various types of intractable seizures, severe to profound psychomotor developmental delay, and mild facial dysmorphism that has_material_basis_in heterozygous mutation in the CYFIP2 gene on chromosome 5q33.]