MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Verloove Vanhorick-Brubakk syndrome

ORPHA:3429Мальформация

Vernal keratoconjunctivitis

ORPHA:70476Заболевание
Not applicable

Verrucous hemangioma

ORPHA:464318Заболевание
Not applicable

Very long chain acyl-CoA dehydrogenase deficiency

ORPHA:26793Заболевание
Autosomal recessive

Vestibular schwannoma

ORPHA:252175Клин. подтип

Vibratory urticaria

ORPHA:493342Заболевание
Autosomal dominant

Vici syndrome

ORPHA:1493Мальформация
Autosomal recessive

Viral hemorrhagic fever

ORPHA:341Категория
Not applicable

Viral myositis

ORPHA:206991Заболевание

Virus-associated trichodysplasia spinulosa

ORPHA:228379Заболевание
Not applicable

Visceral arteriovenous malformation

ORPHA:693855Клин. группа
Not applicable

Visceral heterotaxy

ORPHA:450Категория
Autosomal dominant, Autosomal recessive, X-linked recessive

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

ORPHA:73246Мальформация
Autosomal recessive

Visual snow syndrome

ORPHA:420556Заболевание
Not applicable

Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Заболевание
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Клин. подтип
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Клин. подтип
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Клин. подтип
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia

ORPHA:27Заболевание
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Клин. подтип
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Клин. подтип
Autosomal recessive

Vitamin K antagonist embryofetopathy

ORPHA:1914Мальформация
Not applicable

Vocal cord and pharyngeal distal myopathy

ORPHA:600Заболевание
Autosomal dominant

Vogt-Koyanagi-Harada disease

ORPHA:3437Заболевание
Multigenic/multifactorial