Experimental Factor Ontology
728 terms(s) returned
| Term Type: | Record: 1 to 50 of 728 Records | Page: 1 of 15, First Previous Next Last | Show Records Per Page |
- IFAP syndrome
- IFAP syndrome 1, with or without BRESHECK syndrome
- IFAP syndrome 2
- IFIH1-related type 1 interferonopathy
- IFT140-related recessive ciliopathy
- IKBKG-related immunodeficiency with or without ectodermal dysplasia
- IL10-related early-onset 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
- IRVAN syndrome
- ITM2B amyloidosis
- IVIC syndrome
- IgA nephropathy, susceptibility to
- IgAD1
- IgE responsiveness, atopic
- IgG4-related dacryoadenitis and sialadenitis
- IgG4-related ophthalmic disorder
- IgG4-related retroperitoneal fibrosis
- Imagawa-Matsumoto syndrome
- Imerslund-Grasbeck syndrome
- Imerslund-Grasbeck syndrome type 2
- Ito hypomelanosis
- iatrogenic
- iatrogenic Creutzfeldt-Jakob disease
- iatrogenic botulism
- iatrogenic disease
- iatrogenic or non-iatrogenic
- ichthyosiform erythroderma, corneal involvement, and hearing loss
- ichthyosis
- ichthyosis histrix, Lambert type
- ichthyosis hystrix
- ichthyosis hystrix of Curth-Macklin
- ichthyosis linearis circumflexa
- ichthyosis prematurity syndrome
- ichthyosis vulgaris
- ichthyosis with erythrokeratoderma
- ichthyosis, annular epidermolytic 1
- ichthyosis, annular epidermolytic, 2
- ichthyosis, congenital, autosomal recessive 12
- ichthyosis, congenital, autosomal recessive 13
- ichthyosis, congenital, autosomal recessive 14
