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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

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 thrombocytopenia

ORPHA:3002Ауру
Not applicable

Immune-mediated necrotizing myopathy

ORPHA:206569Ауру
Not applicable

Immune-mediated scleritis

ORPHA:648681Ауру

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

Immunodeficiency due to a late component of complement deficiency

ORPHA:169150Ауру
Autosomal recessive

Immunodeficiency due to ficolin3 deficiency

ORPHA:331190Ауру
Autosomal recessive

Immunodeficiency due to selective anti-polysaccharide antibody deficiency

ORPHA:70593Ауру
Multigenic/multifactorial

Immunodeficiency with factor H anomaly

ORPHA:200421Ауру
Autosomal dominant, Autosomal recessive

Immunodeficiency with factor I anomaly

ORPHA:200418Ауру
Autosomal recessive

Immunodeficiency-congenital thrombocytopenia-hypereosinophilia-colitis-vasculitis syndrome

ORPHA:714496Ауру
Autosomal recessive

Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome

ORPHA:695807Ауру
Autosomal dominant

Immunoglobulin A vasculitis

ORPHA:761Ауру
Not applicable

Immunotactoid glomerulopathy

ORPHA:97567Ауру
Not applicable

Immunotherapy induced hypophysitis

ORPHA:641350Ауру

Incessant infant ventricular tachycardia

ORPHA:45453Ауру
Not applicable

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

ORPHA:52430Ауру
Autosomal dominant

Inclusion body myositis

ORPHA:611Ауру
Not applicable

Indeterminate cell histiocytosis

ORPHA:158019Ауру
Not applicable