All terms in DOID

Label Id Description
cerebral artery UBERON_0004449
prostate calculus DOID_13689
pseudopterygium DOID_11028
patulous eustachian tube DOID_12358 [A eustachian tube disorder with a wider eustachian tube which allows a larger bolus of bacteria-laden material from the nasopharynx during an infection to enter the middle ear, causing a more fulminant infection.]
viral labyrinthitis DOID_12357 [A labyrinthitis which involves viral infection of the inner ear through the upper airway or the blood stream. The symptoms may include hearing loss and ringing in the ears. If the virus reaches the vestibular system, dizziness, severe vertigo with nausea and vomiting, and imbalance can occur.]
mucopolysaccharidosis Ih/s DOID_0111389 [A mucopolysaccharidosis I characterized by an intermediate severity of symptoms including short stature, corneal clouding, joint stiffening, umbilical hernia, dysostosis multiplex, hepatosplenomegaly, and little to no intellectual dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in the IDUA gene on chromosome 4p16.3.]
amelogenesis imperfecta type 1E DOID_0110058 [An amelogenesis imperfecta that has_material_basis_in X-linked dominant mutation in the gene encoding amelogenin (AMELX).]
chronic duodenal ileus DOID_13687
obsolete bacterial prostatitis DOID_12356
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 DOID_0110059 [An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.]
prostatocystitis DOID_12355
familial isolated hypoparathyroidism DOID_0111387 [A hypoparathyroidism characterized by by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects.]
hypoparathyroidism DOID_11199 [A parathyroid gland disease characterized by decreased function of parathyroid glands with underproduction of parathyroid hormone (PTH), leading to abnormally low ionized calcium levels in the blood.]
amelogenesis imperfecta type 1C DOID_0110056 [An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM).]
X-linked hypoparathyroidism DOID_0111388 [A hypoparathyroidism that has_material_basis_in mutation in a region on chromosome Xq27.1 that appears to alter expression of SOX3.]
amelogenesis imperfecta type 2A1 DOID_0110057 [An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13.]
measles DOID_8622 [A viral infectious disease that results_in infection located_in skin, has_material_basis_in Measles virus (Morbillivirus hominis), which is transmitted_by contact with oronasal secretions, or semen of an infected person. The infection has_symptom fever, has_symptom cough, has_symptom coryza, has_symptom conjunctivitis, and has_symptom maculopapular, erythematous rash.]
obsolete reticulosarcoma involving intrapelvic lymph nodes DOID_8620
obsolete postherpetic trigeminal neuralgia DOID_8625 [A viral infectious disease that results_in pain located_in trigeminal nerve, has_material_basis_in Human herpesvirus 3, which reactivates after the initial infection. The infection has_symptom facial pain.]
periostitis DOID_9957 [A connective tissue disease characterized by inflammation located_in the periosteum of the bone.]