All terms in DOID

Label Id Description
neonatal thyrotoxicosis DOID_12573
plethora of newborn DOID_11242
appendiceal neoplasm DOID_11240
phacolytic glaucoma DOID_12570 [A phacogenic glaucoma that is characterized by acute onset of open-angle glaucoma secondary to a leaking mature or hypermature cataract and has_symptom chronic progressive vision loss with acute onset of pain, redness, and blurry vision. Phacolytic glaucomas are caused by direct obstruction of aqueous outflow pathways from leaking cataractous lens proteins.]
polyploid cell CL_0000412
vitamin K deficiency bleeding DOID_11249 [A nutritional deficiency disease that is characterized by easy bleeding due to an inability to form blood clots caused by vitamin K deficiency, occurs most commonly in newborns, and has_material_basis_in deficiency of vitamin K secondary to liver prematurity, lack of vitamin K in a breastmilk diet, largely sterile gut, malabsorption, diarrhea, chronic illness, menorrhagia, chronic kidney disease, and some medications.]
disseminated intravascular coagulation DOID_11247
obsolete hemorrhagic disease of newborn DOID_11248
urethral obstruction DOID_12577
DIC in newborn DOID_11246
anemia of prematurity DOID_11243 [A neonatal anemia that is characterized by anemia experienced by preterm infants in the early postnatal weeks.]
Zaire ebolavirus NCBITaxon_186538
Orthoebolavirus zairense NCBITaxon_3052462
Abnormal atrioventricular valve physiology HP_0031650
orthostatic proteinuria DOID_9617
Marburgvirus NCBITaxon_186537
anterior scleritis DOID_13794
Charcot-Marie-Tooth disease type 4D DOID_0110186 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the N-myc downstream-regulated gene-1 (NDRG1) on chromosome 8q24.]
carp food product FOODON_00001684
Charcot-Marie-Tooth disease type 4K DOID_0110187 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SURF1 gene on chromosome 9q34.]