All terms in DOID

Label Id Description
inflamed seborrheic keratosis DOID_11685
melanoacanthoma DOID_11684
breast fibroadenosis DOID_10352 [A breast benign neoplasm that has_material_basis_in fibrous tissue and epithelial tissue in which tumor cells form glands or glandlike structures.]
pulmonary consolidation SYMP_0000729 [A respiratory system and chest symptom that is characterized by a region of normally compressible lung tissue that has filled with liquid instead of air.]
fibrosclerosis of breast DOID_10353 [A non-proliferative fibrocystic change of the breast that contains scar tissue.]
obsolete glaucoma associated with systemic syndromes DOID_11683
obsolete recurrent malignant pleural mesothelioma DOID_7473
Functional abnormality of the middle ear HP_0011452
malignant pleural mesothelioma DOID_7474 [A pleural cancer that has_material_basis_in mesothelium cells.]
respiratory system cancer DOID_0050615 [An organ system cancer located_in the respiratory system that is characterized by uncontrolled cellular proliferation in the respiratory tract.]
obsolete deep penetrating nevus DOID_7471
obsolete recurrent nevus DOID_7472
diverticulitis DOID_7475 [An intestinal disease characterized by the formation and inflammation of diverticula within the bowel wall.]
nephrotic syndrome type 16 DOID_0080272 [A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.]
microangiopathic hemolytic anemia SYMP_0000720
polycystic kidney disease 5 DOID_0080273 [A autosomal recessive polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of homozygous mutation in the DZIP1L gene on chromosome 3q22.]
duodenal somatostatinoma DOID_7479
duodenum cancer DOID_10021 [A small intestine cancer that is located_in the beginning section of the small intestine.]
nasal cavity carcinoma in situ DOID_6148 [An in situ carcinoma that is located_in the nasal cavity.]
multiple mitochondrial dysfunctions syndrome 5 DOID_0080274 [A multiple mitochondrial dysfunctions syndrome that is characterized by progressive neurologic deterioration beginning in early infancy, with affected individuals having no psychomotor development and early-onset seizures with neurologic decline and spasticity, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the iron-sulfur cluster assembly 1 gene on chromosome 9q21.]