Infantile-onset autosomal recessive nonprogressive cerebellar ataxia

Autosomal recessive

Infancy, Neonatal

Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome

Autosomal recessive

Infancy

Infantile-onset generalized dyskinesia with orofacial involvement

Autosomal recessive

Infancy

Infantile-onset inflammatory bowel disease-hearing loss-recurrent infections syndrome

Autosomal dominant

Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

Autosomal recessive

Infancy, Neonatal

Infantile-onset periodic fever-panniculitis-dermatosis syndrome

Autosomal recessive

Infancy, Neonatal

Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia

Autosomal dominant

Infancy

Infantile-onset spinocerebellar ataxia

Autosomal recessive

Infancy

Infection-related hemolytic uremic syndrome

Not applicable

All ages

Infectious anterior uveitis

All ages

Infectious panuveitis

All ages

Infectious posterior uveitis

All ages

Infective dermatitis associated with HTLV-1

Not applicable

Childhood

Infective endocarditis

All ages

Inflammatory bowel disease-autoimmunity-sinopulmonary infections-lymphadenopathy syndrome

Autosomal dominant

Inflammatory breast cancer

Inflammatory myofibroblastic tumor

Inflammatory myopathy with abundant macrophages

Not applicable

Inflammatory pseudotumor of the liver

Not applicable

All ages

Inhalational anthrax

Not applicable

All ages

Inherited Creutzfeldt-Jakob disease

Autosomal dominant

Adult, Elderly

Inherited acute myeloid leukemia

Autosomal dominant

Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations

Autosomal recessive

Inherited congenital spastic tetraplegia

Autosomal recessive, Unknown

Infancy, Neonatal