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

Intermediate uveitis

ORPHA:279914Kr.
Not applicable

Intermittent hydrarthrosis

ORPHA:329967Kr.

Interstitial cystitis

ORPHA:37202Kr.
Unknown

Interstitial granulomatous dermatitis with arthritis

ORPHA:79099Kr.
Not applicable

Interstitial lung disease due to ABCA3 deficiency

ORPHA:440402Kr.
Autosomal recessive

Interstitial lung disease due to SP-C deficiency

ORPHA:440392Kr.
Autosomal dominant

Interstitial lung disease-brain calcification syndrome

ORPHA:178506Kr.
Autosomal recessive

Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome

ORPHA:306504Kr.
Autosomal recessive

Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency

ORPHA:314376Kr.
Autosomal recessive

Intraductal papillary mucinous carcinoma of pancreas

ORPHA:424058Kr.
Not applicable

Intraductal tubulopapillary neoplasm of pancreas

ORPHA:580572Kr.

Intrahepatic cholestasis of pregnancy

ORPHA:69665Kr.
Multigenic/multifactorial, Not applicable

Intraneural perineurioma

ORPHA:100003Kr.

Intraocular medulloepithelioma

ORPHA:268139Kr.
Not applicable

Intraoral basal cell carcinoma

ORPHA:667678Kr.
Not yet documented

Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome

ORPHA:508512Kr.
Autosomal recessive

Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome

ORPHA:436144Kr.
Autosomal dominant

Intravascular large B-cell lymphoma

ORPHA:98839Kr.
Not applicable

Invasive candidiasis

ORPHA:636945Kr.

Invasive mole

ORPHA:99925Kr.
Not applicable

Invasive non-typhoidal salmonellosis

ORPHA:324648Kr.

Invasive scopulariopsis infection

ORPHA:633124Kr.

Iridocorneal endothelial syndrome

ORPHA:64734Kr.
Not applicable

Isaacs syndrome

ORPHA:84142Kr.
Not applicable