Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
Autosomal recessive
Infancy, Neonatal
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
X-linked recessive
Infancy, Neonatal
Immune thrombocytopenia
Not applicable
All ages
Immune-mediated necrotizing myopathy
Not applicable
Adolescent, Adult, Childhood, Elderly
Immune-mediated scleritis
All ages
Immunodeficiency by defective expression of MHC class I
Autosomal recessive
Childhood
Immunodeficiency by defective expression of MHC class II
Autosomal recessive
Infancy, Neonatal
Immunodeficiency due to CD25 deficiency
Autosomal recessive
Infancy
Immunodeficiency due to MASP-2 deficiency
Autosomal recessive
Adolescent
Immunodeficiency due to a classical component pathway complement deficiency
Autosomal recessive
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
Immunotactoid glomerulopathy
Not applicable
Adult
Immunotherapy induced hypophysitis
All ages
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
Indeterminate cell histiocytosis
Not applicable