All terms in DOID

Label Id Description
malignant growth hormone secreting neoplasm of pituitary DOID_6256
supraglottis squamous cell carcinoma DOID_7587
obsolete mixed endodermal sinus neoplasm and teratoma of the testis DOID_7588
chromophil adenoma of the kidney DOID_6257
supraglottis verrucous carcinoma DOID_7586
growth hormone secreting pituitary adenoma DOID_6255
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.]
obsolete ovarian dermoid cyst with melanocytic nevus DOID_7589
type 1 papillary adenoma of the kidney DOID_6258
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.]
nephrotic syndrome type 5 DOID_0080380 [A familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p.]
nephrotic syndrome type 13 DOID_0080381 [A familial nephrotic syndrome characterized by early onset of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis that has_material_basis_in homozygous mutation in the NUP205 gene on chromosome 7q33.]
patellar tendinitis DOID_10471
tendinitis DOID_971
motor paralysis SYMP_0000848 [A paralysis that is characterized by a complete or partial loss of function the voluntary muscles.]
obsolete candidal pneumonia DOID_10472 [A candidiasis that involves inflammation of the lung caused by Candida species either by hematogenous dissemination or by bronchial extension in patients with oropharyngeal candidiasis. The symptoms include fever, tachypnea, dyspnea, and chest pain.]