Immunodeficiency due to a late component of complement deficiency

Autosomal recessive

Immunodeficiency due to ficolin3 deficiency

Autosomal recessive

Childhood

Immunodeficiency due to selective anti-polysaccharide antibody deficiency

Multigenic/multifactorial

Adolescent, Adult, Childhood

Immunodeficiency with factor H anomaly

Autosomal dominant, Autosomal recessive

Immunodeficiency with factor I anomaly

Autosomal recessive

Adolescent, Adult, Childhood

Immunodeficiency-congenital thrombocytopenia-hypereosinophilia-colitis-vasculitis syndrome

Autosomal recessive

Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome

Autosomal dominant

Immunoglobulin A vasculitis

Not applicable

Childhood

Immunoglobulin-mediated membranoproliferative glomerulonephritis

Multigenic/multifactorial, Unknown

Immunotactoid glomerulopathy

Not applicable

Adult

Immunotactoid or fibrillary glomerulopathy

Not applicable

Adult

Immunotherapy induced hypophysitis

All ages

Imperforate oropharynx-costovertebral anomalies syndrome

Neonatal

Incessant infant ventricular tachycardia

Not applicable

Childhood, Infancy

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Autosomal dominant

Adult

Inclusion body myositis

Not applicable

Adult, Elderly

Incomplete congenital stationary night blindness, Schubert-Bornschein type

Autosomal recessive, X-linked recessive

Incontinentia pigmenti

X-linked dominant

Neonatal

Indeterminate cell histiocytosis

Not applicable

Indolent B-cell non-Hodgkin lymphoma

Adult

Indolent systemic mastocytosis

Not applicable

Adult, Elderly

Indomethacin embryofetopathy

Not applicable

Antenatal, Neonatal

Infant botulism

Infancy, Neonatal

Infantile CLN1 disease

Autosomal recessive