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

Whooping cough

ORPHA:1489Kr.

Wild type ABeta2M amyloidosis

ORPHA:85446Kr.
Not applicable

Wild type ATTR amyloidosis

ORPHA:330001Kr.
Not applicable

Wilson disease

ORPHA:905Kr.
Autosomal recessive

Wiskott-Aldrich syndrome

ORPHA:906Kr.
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

Wolcott-Rallison syndrome

ORPHA:1667Kr.
Autosomal recessive

Wolfram syndrome

ORPHA:3463Kr.
Autosomal recessive

Wolfram-like syndrome

ORPHA:411590Kr.
Autosomal dominant

Woodhouse-Sakati syndrome

ORPHA:3464Kr.
Autosomal recessive

Woolly hair

ORPHA:170Kr.
Autosomal dominant, Autosomal recessive

Woolly hair nevus

ORPHA:79414Kr.
Not applicable

Woolly hair-palmoplantar keratoderma syndrome

ORPHA:420686Kr.
Autosomal recessive

Worster-Drought syndrome

ORPHA:3465Kr.
Autosomal dominant, Not applicable

Wound myiasis

ORPHA:165955Kr.
Not applicable

X-linked Charcot-Marie-Tooth disease type 1

ORPHA:101075Kr.
X-linked dominant

X-linked Charcot-Marie-Tooth disease type 2

ORPHA:101076Kr.
X-linked recessive

X-linked Charcot-Marie-Tooth disease type 3

ORPHA:101077Kr.
X-linked recessive

X-linked Charcot-Marie-Tooth disease type 4

ORPHA:101078Kr.
X-linked recessive

X-linked Charcot-Marie-Tooth disease type 5

ORPHA:99014Kr.
X-linked recessive

X-linked Charcot-Marie-Tooth disease type 6

ORPHA:352675Kr.
X-linked dominant

X-linked Ehlers-Danlos syndrome

ORPHA:75497Kr.
X-linked recessive

X-linked acrogigantism

ORPHA:300373Kr.
X-linked dominant

X-linked adrenal hypoplasia congenita

ORPHA:95702Kr.
X-linked recessive

X-linked adrenoleukodystrophy

ORPHA:43Kr.
X-linked dominant