MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

IgG4-related sclerosing cholangitis

ORPHA:447764Клин. под.
Not applicable

IgG4-related submandibular gland disease

ORPHA:449432Клин. под.
Not applicable

IgG4-related systemic disease

ORPHA:596448Ауру
Not applicable

IgG4-related thyroid disease

ORPHA:64744Клин. под.
Not applicable

Ileal neuroendocrine tumor

ORPHA:100078Ауру
Not applicable

Ileal pouch anal anastomosis related faecal incontinence

ORPHA:238621Жағдай
Not applicable

Imagawa-Matsumoto syndrome

ORPHA:659463Мальф.
Autosomal dominant

Imerslund-Gräsbeck syndrome

ORPHA:35858Ауру
Autosomal recessive

Iminoglycinuria

ORPHA:42062Ауру
Autosomal recessive

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590Ауру
Autosomal recessive

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

ORPHA:529980Ауру

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

ORPHA:238569Ауру
Autosomal recessive

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

ORPHA:529977Ауру
Autosomal recessive

Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

ORPHA:37042Ауру
X-linked recessive

Immune hydrops fetalis

ORPHA:364013Клин. под.
Not applicable

Immune thrombocytopenia

ORPHA:3002Ауру
Not applicable

Immune-mediated necrotizing myopathy

ORPHA:206569Ауру
Not applicable

Immune-mediated scleritis

ORPHA:648681Ауру

Immune-mediated thrombotic thrombocytopenic purpura

ORPHA:93585Клин. под.
Multigenic/multifactorial

Immunodeficiency by defective expression of MHC class I

ORPHA:34592Ауру
Autosomal recessive

Immunodeficiency by defective expression of MHC class II

ORPHA:572Ауру
Autosomal recessive

Immunodeficiency due to CD25 deficiency

ORPHA:169100Ауру
Autosomal recessive

Immunodeficiency due to MASP-2 deficiency

ORPHA:331187Ауру
Autosomal recessive

Immunodeficiency due to a classical component pathway complement deficiency

ORPHA:169147Ауру
Autosomal recessive