MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Idiopathic pulmonary fibrosis

ORPHA:2032Kr.
Multigenic/multifactorial

Idiopathic pulmonary hemosiderosis

ORPHA:99931Kr.

Idiopathic recurrent pericarditis

ORPHA:251307Kr.
Not applicable

Idiopathic recurrent stupor

ORPHA:276174Kr.
Not applicable

Idiopathic spontaneous coronary artery dissection

ORPHA:458718Kr.
Not applicable

Idiopathic steroid-resistant nephrotic syndrome

ORPHA:567548Clinical syndrome

Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy

ORPHA:567552Kl. subt.

Idiopathic steroid-sensitive nephrotic syndrome

ORPHA:69061Clinical syndrome
Unknown

Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance

ORPHA:567546Clinical syndrome

Idiopathic trachyonychia

ORPHA:79153Kr.
Autosomal dominant

Idiopathic triglyceride deposit cardiomyovasculopathy

ORPHA:692296Ätl. subt.
Unknown

Idiopathic uveal effusion syndrome

ORPHA:209956Kr.
Unknown

Idiopathic ventricular fibrillation

ORPHA:228140Kr.
Autosomal dominant, Not applicable

Idiopathic/heritable pulmonary arterial hypertension

ORPHA:422Kr.
Autosomal dominant, Autosomal recessive, Not applicable

IgA pemphigus

ORPHA:555905Kr.

IgG4-related aortitis

ORPHA:449400Kl. subt.
Not applicable

IgG4-related dacryoadenitis and sialadenitis

ORPHA:79078Kl. subt.
Not applicable

IgG4-related disease

ORPHA:284264Kl. gruppe
Not applicable

IgG4-related kidney disease

ORPHA:449395Kl. subt.
Not applicable

IgG4-related mediastinitis

ORPHA:63999Kl. subt.
Not applicable

IgG4-related mesenteritis

ORPHA:238593Kl. subt.
Not applicable

IgG4-related ophthalmic disease

ORPHA:449563Kl. subt.
Not applicable

IgG4-related pachymeningitis

ORPHA:449427Kl. subt.
Not applicable

IgG4-related retroperitoneal fibrosis

ORPHA:49041Kl. subt.
Not applicable, Unknown