Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
IgG4-related sclerosing cholangitis
Not applicable
IgG4-related submandibular gland disease
Not applicable
Adult, Elderly
IgG4-related systemic disease
Not applicable
Adolescent, Adult, Childhood, Elderly
IgG4-related thyroid disease
Not applicable
Adult
Ileal neuroendocrine tumor
Not applicable
Adult
Ileal pouch anal anastomosis related faecal incontinence
Not applicable
All ages
Imagawa-Matsumoto syndrome
Autosomal dominant
Antenatal, Neonatal
Imerslund-Gräsbeck syndrome
Autosomal recessive
Childhood
Iminoglycinuria
Autosomal recessive
All ages
Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency
Autosomal recessive
Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome
Infancy
Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome
Autosomal recessive
Infancy, Neonatal
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 hydrops fetalis
Not applicable
Antenatal, Neonatal
Immune thrombocytopenia
Not applicable
All ages
Immune-mediated necrotizing myopathy
Not applicable
Adolescent, Adult, Childhood, Elderly
Immune-mediated scleritis
All ages
Immune-mediated thrombotic thrombocytopenic purpura
Multigenic/multifactorial
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