MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 727 заболеваний (Клин. под.) Қалпына келтіру

Vestibular schwannoma

ORPHA:252175Клин. под.

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Клин. под.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Клин. под.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Клин. под.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Клин. под.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Клин. под.
Autosomal recessive

Von Willebrand disease type 1

ORPHA:166078Клин. под.
Autosomal dominant

Von Willebrand disease type 2

ORPHA:166081Клин. под.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2A

ORPHA:166084Клин. под.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2B

ORPHA:166087Клин. под.
Autosomal dominant

Von Willebrand disease type 2M

ORPHA:166090Клин. под.
Autosomal dominant

Von Willebrand disease type 2N

ORPHA:166093Клин. под.
Autosomal recessive

Von Willebrand disease type 3

ORPHA:166096Клин. под.
Autosomal recessive

Waardenburg syndrome type 1

ORPHA:894Клин. под.
Autosomal dominant

Waardenburg syndrome type 2

ORPHA:895Клин. под.
Autosomal dominant

Waardenburg syndrome type 3

ORPHA:896Клин. под.
Autosomal dominant, Autosomal recessive

Wolman disease

ORPHA:75233Клин. под.
Autosomal recessive

Wrinkly skin syndrome

ORPHA:2834Клин. под.
Autosomal recessive

X-linked Alport syndrome

ORPHA:88917Клин. под.
X-linked dominant

X-linked Alport syndrome-diffuse leiomyomatosis

ORPHA:1018Клин. под.
X-linked dominant

X-linked agammaglobulinemia

ORPHA:47Клин. под.
X-linked recessive

X-linked cerebral adrenoleukodystrophy

ORPHA:139396Клин. под.
X-linked recessive

X-linked complicated corpus callosum dysgenesis

ORPHA:1497Клин. под.
X-linked recessive

X-linked complicated spastic paraplegia type 1

ORPHA:306617Клин. под.
X-linked recessive