All terms in DOID

Label Id Description
glottis verrucous carcinoma DOID_7583
glottis squamous cell carcinoma DOID_7031 [A squamous cell carcinoma that is located_in the glottis.]
subglottis verrucous carcinoma DOID_7584
subglottis squamous cell carcinoma DOID_7585
obsolete psychogenic depressive psychosis DOID_7581
obsolete Epstein-Barr virus related carcinoma DOID_6250 [An Epstein-Barr virus infectious disease and is_a carcinoma that derives_from epithelial cells, has_material_basis_in Human herpesvirus 4, which causes a growth activation of the epithelial cells that it infects.]
supraglottis squamous cell carcinoma DOID_7587
malignant growth hormone secreting neoplasm of pituitary DOID_6256
obsolete mixed endodermal sinus neoplasm and teratoma of the testis DOID_7588
chromophil adenoma of the kidney DOID_6257
growth hormone secreting pituitary adenoma DOID_6255
supraglottis verrucous carcinoma DOID_7586
nephrotic syndrome type 3 DOID_0080382 [A familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has_material_basis_in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23.]
phantom pain SYMP_0000830 [A pain that is characterized by a painful sensation that is perceived to originate in the amputated portion of the extremety. Patients may have localized pain that originates in the stump.]
nephrotic syndrome type 4 DOID_0080383 [A familial nephrotic syndrome that has_material_basis_in heterozygous mutation in the WT1 gene on chromosome 11p13.]
type 1 papillary adenoma of the kidney DOID_6258
obsolete ovarian dermoid cyst with melanocytic nevus DOID_7589
nephrotic syndrome type 6 DOID_0080384 [A familial nephrotic syndrome that has_material_basis_in homozygous mutation in the PTPRO gene on chromosome 12p12.]
type 2 papillary adenoma of the kidney DOID_6259
nephrotic syndrome type 11 DOID_0080385 [A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15.]