MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Verloove Vanhorick-Brubakk syndrome

ORPHA:3429Malf.

Vernal keratoconjunctivitis

ORPHA:70476Kr.
Not applicable

Verrucous hemangioma

ORPHA:464318Kr.
Not applicable

Very long chain acyl-CoA dehydrogenase deficiency

ORPHA:26793Kr.
Autosomal recessive

Vestibular schwannoma

ORPHA:252175Kl. subt.

Vibratory urticaria

ORPHA:493342Kr.
Autosomal dominant

Vici syndrome

ORPHA:1493Malf.
Autosomal recessive

Viral hemorrhagic fever

ORPHA:341Kat.
Not applicable

Viral myositis

ORPHA:206991Kr.

Virus-associated trichodysplasia spinulosa

ORPHA:228379Kr.
Not applicable

Visceral arteriovenous malformation

ORPHA:693855Kl. gruppe
Not applicable

Visceral heterotaxy

ORPHA:450Kat.
Autosomal dominant, Autosomal recessive, X-linked recessive

Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome

ORPHA:73246Malf.
Autosomal recessive

Visual snow syndrome

ORPHA:420556Kr.
Not applicable

Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Kr.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Kl. subt.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Kl. subt.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Kl. subt.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia

ORPHA:27Kr.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Kl. subt.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Kl. subt.
Autosomal recessive

Vitamin K antagonist embryofetopathy

ORPHA:1914Malf.
Not applicable

Vocal cord and pharyngeal distal myopathy

ORPHA:600Kr.
Autosomal dominant

Vogt-Koyanagi-Harada disease

ORPHA:3437Kr.
Multigenic/multifactorial