MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

VACTERL/VATER association

ORPHA:887Мальформация
Not applicable

VEXAS syndrome

ORPHA:596753Заболевание
Not applicable

VIPoma

ORPHA:97282Заболевание
Not applicable

VPS11-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:466934Заболевание
Autosomal recessive

Vacuolar myopathy with sarcoplasmic reticulum protein aggregates

ORPHA:88635Заболевание
Autosomal dominant, Unknown

Vaginal atresia

ORPHA:65681Морф. аномалия
Not applicable

Vaginal carcinoma

ORPHA:180247Заболевание

Van den Ende-Gupta syndrome

ORPHA:2460Мальформация
Autosomal recessive

Van der Woude syndrome

ORPHA:888Мальформация
Autosomal dominant, Not applicable

Variably protease-sensitive prionopathy

ORPHA:454742Заболевание
Not applicable

Variant ABeta2M amyloidosis

ORPHA:314652Заболевание
Autosomal dominant

Variant Creutzfeldt-Jakob disease

ORPHA:576370Заболевание

Variant of Guillain-Barré syndrome

ORPHA:231413Категория
Multigenic/multifactorial, Not applicable

Variegate porphyria

ORPHA:79473Заболевание
Autosomal dominant

Vascular Ehlers-Danlos syndrome

ORPHA:286Заболевание
Autosomal dominant, Autosomal recessive

Vascular Ehlers-Danlos-polymicrogyria syndrome

ORPHA:636941Заболевание

Vasculitis

ORPHA:52759Категория

Vegetative pyoderma gangrenosum

ORPHA:538872Клин. подтип
Multigenic/multifactorial

Vein of Galen malformation

ORPHA:1053Морф. аномалия
Not applicable

Velo-facial-skeletal syndrome

ORPHA:3424Мальформация

Venezuelan hemorrhagic fever

ORPHA:319234Заболевание

Ventilator-induced diaphragmatic dysfunction

ORPHA:505395Особая клин. ситуация

Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome

ORPHA:3201Мальформация
Unknown

Ventriculomegaly-cystic kidney disease

ORPHA:443988Заболевание
Autosomal recessive