MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Ulnar hypoplasia-split foot syndrome

ORPHA:1122Malf.

Ulnar-mammary syndrome

ORPHA:3138Malf.
Autosomal dominant

Ulnar/fibula ray defect-brachydactyly syndrome

ORPHA:52056Malf.
Autosomal dominant

Umbilical cord ulceration-intestinal atresia syndrome

ORPHA:3405Malf.
Unknown

Unclassified acute myeloid leukemia

ORPHA:167714Kat.

Unclassified autoinflammatory syndrome

ORPHA:324936Kat.

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.

Unicentric Castleman disease

ORPHA:93685Kl. subt.

Unifocal Langerhans cell histiocytosis

ORPHA:687730Kl. subt.
Not applicable

Unilateral focal polymicrogyria

ORPHA:268947Kl. subt.

Unilateral hemispheric polymicrogyria

ORPHA:101071Kl. subt.

Unilateral multicystic dysplastic kidney

ORPHA:97363Kl. subt.
Autosomal dominant

Unilateral ocular duplication

ORPHA:3374Morph.
Autosomal dominant

Unilateral polymicrogyria

ORPHA:268943Morph.

Univentricular heart

ORPHA:1464Morph.
Not applicable

Unspecified juvenile idiopathic arthritis

ORPHA:91140Kr.