MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Woolly hair nevus

ORPHA:79414Kr.
Not applicable

Woolly hair-palmoplantar keratoderma syndrome

ORPHA:420686Kr.
Autosomal recessive

Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia

ORPHA:166277Malf.
Unknown

Wormian bones-micrognathia-abnormal dentition-progeroid syndrome

ORPHA:659873Malf.
Autosomal dominant

Worster-Drought syndrome

ORPHA:3465Kr.
Autosomal dominant, Not applicable

Wound botulism

ORPHA:178475Ätl. subt.

Wound myiasis

ORPHA:165955Kr.
Not applicable

Wrinkly skin syndrome

ORPHA:2834Kl. subt.
Autosomal recessive

X small rings syndrome

ORPHA:96201Malf.

X-linked Alport syndrome

ORPHA:88917Kl. subt.
X-linked dominant

X-linked Alport syndrome-diffuse leiomyomatosis

ORPHA:1018Kl. subt.
X-linked dominant

X-linked Charcot-Marie-Tooth disease

ORPHA:64747Kl. gruppe
X-linked dominant, X-linked recessive

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 Emery-Dreifuss muscular dystrophy

ORPHA:98863Ätl. subt.
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

X-linked agammaglobulinemia

ORPHA:47Kl. subt.
X-linked recessive