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

Idiopathic macular telangiectasia type 1

ORPHA:353344Kr.

Idiopathic macular telangiectasia type 3

ORPHA:353351Kr.

Idiopathic neonatal atrial flutter

ORPHA:45452Kr.
Not applicable

Idiopathic panuveitis

ORPHA:280921Kr.
Not applicable

Idiopathic peliosis hepatis

ORPHA:480524Kr.

Idiopathic phalangeal acro-osteolysis

ORPHA:444316Kr.
Not applicable

Idiopathic pleuroparenchymal fibroelastosis

ORPHA:494428Kr.

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 trachyonychia

ORPHA:79153Kr.
Autosomal dominant

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 systemic disease

ORPHA:596448Kr.
Not applicable

Ileal neuroendocrine tumor

ORPHA:100078Kr.
Not applicable

Imerslund-Gräsbeck syndrome

ORPHA:35858Kr.
Autosomal recessive

Iminoglycinuria

ORPHA:42062Kr.
Autosomal recessive

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590Kr.
Autosomal recessive

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

ORPHA:529980Kr.

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

ORPHA:238569Kr.
Autosomal recessive