All terms in DOID

Label Id Description
prion NCBITaxon_36469
acrylamide CHEBI_28619 [A member of the class of acrylamides that results from the formal condensation of acrylic acid with ammonia.]
mechanosensory system UBERON_0007037
sensory system UBERON_0001032
Betacoronavirus cameli NCBITaxon_3433633
Merbecovirus NCBITaxon_2509494
Monjiviricetes NCBITaxon_2497574
Abnormal granulocyte morphology HP_0001911
Abnormal myeloid leukocyte morphology HP_0010974
mucopolysaccharidosis III DOID_12801 [A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain.]
mucopolysaccharidosis DOID_12798 [A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine.]
mucopolysaccharidosis VI DOID_12800 [A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase.]
susceptibility to Graves disease X-linked 1 MIM_300351
chronic lacrimal gland enlargement DOID_12809
dacryoadenitis DOID_950
Hepatitis delta virus NCBITaxon_12475
Deltavirus italiense NCBITaxon_2844074
mucopolysaccharidosis IV DOID_12804 [A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain.]
mucopolysaccharidosis type VII DOID_12803 [A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme beta-glucuronidase resulting in the inability to degrade glucuronic acid-containing glycosaminoglycans.]
mucopolysaccharidosis I DOID_12802 [A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme alpha-L-iduronidase.]