MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
727 diseases matched (Clin. sub.) Reset

Vestibular schwannoma

ORPHA:252175Clin. sub.

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Clin. sub.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Clin. sub.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Clin. sub.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Clin. sub.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Clin. sub.
Autosomal recessive

Von Willebrand disease type 1

ORPHA:166078Clin. sub.
Autosomal dominant

Von Willebrand disease type 2

ORPHA:166081Clin. sub.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2A

ORPHA:166084Clin. sub.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2B

ORPHA:166087Clin. sub.
Autosomal dominant

Von Willebrand disease type 2M

ORPHA:166090Clin. sub.
Autosomal dominant

Von Willebrand disease type 2N

ORPHA:166093Clin. sub.
Autosomal recessive

Von Willebrand disease type 3

ORPHA:166096Clin. sub.
Autosomal recessive

Waardenburg syndrome type 1

ORPHA:894Clin. sub.
Autosomal dominant

Waardenburg syndrome type 2

ORPHA:895Clin. sub.
Autosomal dominant

Waardenburg syndrome type 3

ORPHA:896Clin. sub.
Autosomal dominant, Autosomal recessive

Wolman disease

ORPHA:75233Clin. sub.
Autosomal recessive

Wrinkly skin syndrome

ORPHA:2834Clin. sub.
Autosomal recessive

X-linked Alport syndrome

ORPHA:88917Clin. sub.
X-linked dominant

X-linked Alport syndrome-diffuse leiomyomatosis

ORPHA:1018Clin. sub.
X-linked dominant

X-linked agammaglobulinemia

ORPHA:47Clin. sub.
X-linked recessive

X-linked cerebral adrenoleukodystrophy

ORPHA:139396Clin. sub.
X-linked recessive

X-linked complicated corpus callosum dysgenesis

ORPHA:1497Clin. sub.
X-linked recessive

X-linked complicated spastic paraplegia type 1

ORPHA:306617Clin. sub.
X-linked recessive