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

Tyrosinemia type 2

ORPHA:28378Kr.
Autosomal recessive

Tyrosinemia type 3

ORPHA:69723Kr.
Autosomal recessive

UV-sensitive syndrome

ORPHA:178338Kr.
Autosomal recessive

Ulerythema ophryogenesis

ORPHA:3406Kr.
Autosomal dominant, Not applicable

Ullrich congenital muscular dystrophy

ORPHA:75840Kr.
Autosomal dominant, Autosomal recessive

Unclassified myelodysplastic syndrome

ORPHA:98827Kr.
Not applicable

Unclassified vasculitis

ORPHA:251328Kr.
Not applicable

Uncombable hair syndrome

ORPHA:1410Kr.
Autosomal recessive

Undifferentiated carcinoma of esophagus

ORPHA:418951Kr.
Not applicable

Undifferentiated carcinoma of liver and intrahepatic biliary tract

ORPHA:424970Kr.
Not applicable

Undifferentiated carcinoma of stomach

ORPHA:423786Kr.
Not applicable

Undifferentiated carcinoma with osteoclast-like giant cells of pancreas

ORPHA:424080Kr.
Not applicable

Undifferentiated pleomorphic sarcoma

ORPHA:2023Kr.
Not applicable

Unexplained long-lasting fever/inflammatory syndrome

ORPHA:251332Kr.

Unspecified juvenile idiopathic arthritis

ORPHA:91140Kr.

Unstable alpha globin chain variant disease

ORPHA:707789Kr.
Autosomal dominant

Unstable beta globin chain variant disease

ORPHA:231226Kr.
Autosomal dominant

Unstable gamma globin chain variant disease

ORPHA:707792Kr.
Autosomal dominant

Upper tract urothelial carcinoma

ORPHA:598216Kr.

Urachal carcinoma

ORPHA:695020Kr.
Not applicable

Urocanic aciduria

ORPHA:210128Kr.
Autosomal recessive

Usher syndrome

ORPHA:886Kr.
Autosomal recessive

Uveal melanoma

ORPHA:39044Kr.
Not applicable

VEXAS syndrome

ORPHA:596753Kr.
Not applicable