All terms in DOID

Label Id Description
kaolin pneumoconiosis DOID_10331 [A pneumoconiosis that is caused by inhalation of kaolin dust.]
blue color blindness DOID_11661 [A color blindness that is characterized by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.]
color blindness DOID_13399 [A blindness that is characterized by the inability or decreased ability to see color, or perceive color differences, under normal lighting conditions.]
childhood embryonal testis carcinoma DOID_6162 [An embryonal testis carcinoma that occurs in children.]
familial renal papillary carcinoma DOID_6163
Aplasia/hypoplasia involving the skeleton HP_0009115
obsolete subchronic schizophrenia DOID_10338
prostatic urethra urothelial carcinoma DOID_6166 [A prostatic urethral cancer that derives_from the urothelial lining of the prostatic urethra.]
prostatic urethral cancer DOID_6167 [A male urethral cancer that derives_from the prostatic urethra.]
Aplasia/Hypoplasia involving bones of the skull HP_0009116
Aplasia/hypoplasia affecting bones of the axial skeleton HP_0009122
obsolete schizophrenia simplex DOID_10339
hypertrichosis of eyelid DOID_11669
hypertrichosis DOID_420 [A hair disease characterized by hair growth that is abnormal in quantity or location.]
parametrium UBERON_0010391
mesentery UBERON_0002095
mesometrium UBERON_0003885
male urethral cancer DOID_736 [An urethral cancer that derives_from the male urethra.]
obsolete AIDS-related Human papillomavirus infectious disease DOID_7498 [A papillomavirus infectious disease and complicated_by acquired immunodeficiency syndrome that results_in infection, has_material_basis_in human papillomavirus, in patients with AIDS.]
Charcot-Marie-Tooth disease dominant intermediate G DOID_0080294 [A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21.]