Mondo Disease Ontology
1601 terms(s) returned
| Term Type: | Record: 1 to 50 of 1601 Records | Page: 1 of 33, First Previous Next Last | Show Records Per Page |
- IBR abortion/fetal death, non-human animal
- ICHAD syndrome
- IDH-mutant anaplastic astrocytoma
- IDH-mutant and 1p/19q-codeleted oligodendroglioma
- IDH-wildtype anaplastic astrocytoma
- IDH-wildtype glioblastoma
- IDH3B-related retinopathy
- IFAP syndrome
- IFAP syndrome 1, with or without BRESHECK syndrome
- IFAP syndrome 2
- IFIH1-related hereditary spastic paraplegia
- IFIH1-related type 1 interferonopathy
- IFT140-related recessive ciliopathy
- IKBKG-related immunodeficiency with or without ectodermal dysplasia
- IKZF2-related combined immunodeficiency
- IL10-related early-onset inflammatory bowel disease
- IL21-related infantile inflammatory bowel disease
- IMAGe syndrome
- IMPDH1-related retinopathy
- IMPG1-related dominant retinopathy
- IMPG1-related recessive retinopathy
- IMPG2-related dominant retinopathy
- IMPG2-related recessive retinopathy
- INTU-related skeletal ciliopathy
- IRF4-related combined immunodeficiency
- IRF4-related immune disorder
- IRF6-related condition
- IRIDA syndrome
- IRIS azotemia stage I, non-human animal
- IRIS azotemia stage II, non-human animal
- IRIS azotemia stage III, non-human animal
- IRIS azotemia stage IV, non-human animal
- IRIS blood pressure end-organ damage from hypertension, non-human animal
- IRIS blood pressure low risk, non-human animal
- IRIS blood pressure minimal risk, non-human animal
- IRIS blood pressure moderate risk, non-human animal
- IRIS blood pressure severe risk, non-human animal
- IRIS borderline proteinuric, non-human animal
- IRIS non-proteinuric, non-human animal
- IRIS proteinuric, non-human animal
- IRVAN syndrome
- ITM2B amyloidosis
- ITPKB deficiency
- IVIC syndrome
- IgA glomerulonephritis
- IgA nephropathy, susceptibility to
- IgA nephropathy, susceptibility to, 1
- IgA nephropathy, susceptibility to, 2
- IgA nephropathy, susceptibility to, 3
- IgA pemphigus
