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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

IgG4-related sclerosing cholangitis

ORPHA:447764Clin. sub.
Not applicable

IgG4-related submandibular gland disease

ORPHA:449432Clin. sub.
Not applicable

IgG4-related systemic disease

ORPHA:596448Disease
Not applicable

IgG4-related thyroid disease

ORPHA:64744Clin. sub.
Not applicable

Ileal neuroendocrine tumor

ORPHA:100078Disease
Not applicable

Ileal pouch anal anastomosis related faecal incontinence

ORPHA:238621Situation
Not applicable

Imagawa-Matsumoto syndrome

ORPHA:659463Malform.
Autosomal dominant

Imerslund-Gräsbeck syndrome

ORPHA:35858Disease
Autosomal recessive

Iminoglycinuria

ORPHA:42062Disease
Autosomal recessive

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590Disease
Autosomal recessive

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

ORPHA:529980Disease

Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome

ORPHA:238569Disease
Autosomal recessive

Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome

ORPHA:529977Disease
Autosomal recessive

Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

ORPHA:37042Disease
X-linked recessive

Immune hydrops fetalis

ORPHA:364013Clin. sub.
Not applicable

Immune thrombocytopenia

ORPHA:3002Disease
Not applicable

Immune-mediated necrotizing myopathy

ORPHA:206569Disease
Not applicable

Immune-mediated scleritis

ORPHA:648681Disease

Immune-mediated thrombotic thrombocytopenic purpura

ORPHA:93585Clin. sub.
Multigenic/multifactorial

Immunodeficiency by defective expression of MHC class I

ORPHA:34592Disease
Autosomal recessive

Immunodeficiency by defective expression of MHC class II

ORPHA:572Disease
Autosomal recessive

Immunodeficiency due to CD25 deficiency

ORPHA:169100Disease
Autosomal recessive

Immunodeficiency due to MASP-2 deficiency

ORPHA:331187Disease
Autosomal recessive

Immunodeficiency due to a classical component pathway complement deficiency

ORPHA:169147Disease
Autosomal recessive