MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Verloove Vanhorick-Brubakk syndrome

ORPHA:3429Мальф.

Vernal keratoconjunctivitis

ORPHA:70476Ауру
Not applicable

Verrucous hemangioma

ORPHA:464318Ауру
Not applicable

Very long chain acyl-CoA dehydrogenase deficiency

ORPHA:26793Ауру
Autosomal recessive

Vestibular schwannoma

ORPHA:252175Клин. под.

Vibratory urticaria

ORPHA:493342Ауру
Autosomal dominant

Vici syndrome

ORPHA:1493Мальф.
Autosomal recessive

Viral hemorrhagic fever

ORPHA:341Сан.
Not applicable

Viral myositis

ORPHA:206991Ауру

Virus-associated trichodysplasia spinulosa

ORPHA:228379Ауру
Not applicable

Visceral arteriovenous malformation

ORPHA:693855Клин. топ
Not applicable

Visceral heterotaxy

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

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

ORPHA:73246Мальф.
Autosomal recessive

Visual snow syndrome

ORPHA:420556Ауру
Not applicable

Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Ауру
Autosomal recessive

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

ORPHA:27Ауру
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

Vitamin K antagonist embryofetopathy

ORPHA:1914Мальф.
Not applicable

Vocal cord and pharyngeal distal myopathy

ORPHA:600Ауру
Autosomal dominant

Vogt-Koyanagi-Harada disease

ORPHA:3437Ауру
Multigenic/multifactorial