All terms in DOID

Label Id Description
obsolete opportunistic Campylobacteraceae infectious disease DOID_0050378
renal artery obstruction DOID_2972
female breast lower-inner quadrant cancer DOID_1649 [A female breast cancer that is located_in the lower-inner quadrant of the breast.]
kidney cortex necrosis DOID_2973 [A kidney cortex disease that is characterized by death of the tissue in the outer part of the kidney that results from blockage of the small arteries that supply blood to the cortex and that causes acute kidney injury.]
obsolete multicystic dysplastic kidney DOID_2974
female breast upper-inner quadrant cancer DOID_1647 [A female breast cancer that is located_in the upper-inner quadrant of the breast.]
obsolete glomerular vascular disorder DOID_2976
antiphospholipid syndrome DOID_2988 [An autoimmune disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin).]
obsolete commensal Enterobacteriaceae infectious disease DOID_0050360
obsolete Atypical small acinar proliferation of the prostate gland DOID_2989
obsolete Elizabethkingia meningoseptica infectious disease DOID_0050362
obsolete opportunistic Enterobacteriaceae infectious disease DOID_0050361
obsolete opportunistic Flavobacteriaceae infectious disease DOID_0050364
obsolete Capnocytophaga canimorsus infectious disease DOID_0050363
female breast axillary tail cancer DOID_1650 [A female breast cancer that is located_in the breast tissue extending into the axilla.]
obsolete Empedobacter brevis endophthalmitis DOID_0050366
obsolete Chryseobacterium indologenes infectious disease DOID_0050365
female-restricted Wieacker-Wolff syndrome DOID_0061015 [A syndromic X-linked intellectual disability that has_material_basis_in heterozygous mutation in the ZC4H2 gene on chromosome Xq11.]
autosomal recessive nonsyndromic deafness 61 DOID_0110513 [An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22.]
X-linked intellectual developmental disorder 108 DOID_0111844 [A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3.]