All terms in DOID

Label Id Description
nodular ganglioneuroblastoma DOID_5193
ganglioneuroblastoma DOID_4163
Abnormal nervous system morphology HP_0012639
obsolete non-neoplastic nevus of skin DOID_12860
obsolete recurrent nephroblastoma DOID_5184 [A nephroblastoma that recurs over time.]
hereditary Wilms' tumor DOID_5183 [A nephroblastoma that results_in either bilateral disease or a family history of Wilms' tumour.]
obsolete anaplastic renal Wilms' tumor DOID_5185 [A nephroblastoma that results_in an unfavorable appearance under the microscope. They are characterized by a cell nuclei that tends to be very large and distorted.]
chondroid lipoma DOID_10208 [A lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women.]
extrahepatic bile duct lipoma DOID_10209 [A biliary tract benign neoplasm that is located_in the extrahepatic bile duct and derives_from fat cells.]
lipoma of spermatic cord DOID_10206 [A paratesticular lipoma that is located_in the spermatic cord and derives_from fat cells.]
paratesticular lipoma DOID_10207 [A reproductive organ benign neoplasm that derives_from fat cells located_in the paratesticular region.]
epithelial predominant Wilms' tumor DOID_5189
reproductive organ benign neoplasm DOID_0050622 [An organ system benign neoplasm that is located_in reproductive system organs.]
lupus nephritis DOID_0080162 [A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus.]
otulipenia DOID_0080163 [An immune system disease that is characterized by neonatal onset of recurrent fever, erythematous rash with painful nodules, painful joints, and lipodystrophy and has_material_basis_in autosomal recessive inheritance of homozygous loss-of-function mutations in the OTULIN gene encoding a deubiquitinase with linear linkage specificity on chromosome 5p15.]
myeloid and lymphoid neoplasms associated with PDGFRA rearrangement DOID_0080165 [A myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts.]
Cytomegalovirus retinitis DOID_0080160 [A retinitis that has_material_basis_in Cytomegalovirus.]
cutaneous candidiasis DOID_0080161 [A candidiasis that is characterized by Candida infection located_in the skin.]
Dothideales NCBITaxon_5014
hepatic veno-occlusive disease DOID_0080177 [A hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver.]