MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

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

ORPHA:529977Kr.
Autosomal recessive

Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

ORPHA:37042Kr.
X-linked recessive

Immune thrombocytopenia

ORPHA:3002Kr.
Not applicable

Immune-mediated necrotizing myopathy

ORPHA:206569Kr.
Not applicable

Immune-mediated scleritis

ORPHA:648681Kr.

Immunodeficiency by defective expression of MHC class I

ORPHA:34592Kr.
Autosomal recessive

Immunodeficiency by defective expression of MHC class II

ORPHA:572Kr.
Autosomal recessive

Immunodeficiency due to CD25 deficiency

ORPHA:169100Kr.
Autosomal recessive

Immunodeficiency due to MASP-2 deficiency

ORPHA:331187Kr.
Autosomal recessive

Immunodeficiency due to a classical component pathway complement deficiency

ORPHA:169147Kr.
Autosomal recessive

Immunodeficiency due to a late component of complement deficiency

ORPHA:169150Kr.
Autosomal recessive

Immunodeficiency due to ficolin3 deficiency

ORPHA:331190Kr.
Autosomal recessive

Immunodeficiency due to selective anti-polysaccharide antibody deficiency

ORPHA:70593Kr.
Multigenic/multifactorial

Immunodeficiency with factor H anomaly

ORPHA:200421Kr.
Autosomal dominant, Autosomal recessive

Immunodeficiency with factor I anomaly

ORPHA:200418Kr.
Autosomal recessive

Immunodeficiency-congenital thrombocytopenia-hypereosinophilia-colitis-vasculitis syndrome

ORPHA:714496Kr.
Autosomal recessive

Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome

ORPHA:695807Kr.
Autosomal dominant

Immunoglobulin A vasculitis

ORPHA:761Kr.
Not applicable

Immunotactoid glomerulopathy

ORPHA:97567Kr.
Not applicable

Immunotherapy induced hypophysitis

ORPHA:641350Kr.

Incessant infant ventricular tachycardia

ORPHA:45453Kr.
Not applicable

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

ORPHA:52430Kr.
Autosomal dominant

Inclusion body myositis

ORPHA:611Kr.
Not applicable

Indeterminate cell histiocytosis

ORPHA:158019Kr.
Not applicable