MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Staphylococcal toxemia

ORPHA:300579Категория

Staphylococcal toxic-shock syndrome

ORPHA:99919Этиол. подтип
Not applicable

Stargardt disease

ORPHA:827Заболевание
Autosomal dominant, Autosomal recessive

Steatocystoma multiplex-natal teeth syndrome

ORPHA:3184Мальформация
Autosomal dominant

Steel syndrome

ORPHA:438117Заболевание
Autosomal recessive

Steinert myotonic dystrophy

ORPHA:273Заболевание
Autosomal dominant

Stellate multiform amelanotic choroidopathy

ORPHA:674958Заболевание

Sterile multifocal osteomyelitis with periostitis and pustulosis

ORPHA:210115Заболевание
Autosomal recessive

Sternal cleft

ORPHA:2017Морф. аномалия
Not applicable

Steroid dehydrogenase deficiency-dental anomalies syndrome

ORPHA:3196Заболевание
Autosomal recessive

Steroid-responsive encephalopathy associated with autoimmune thyroiditis

ORPHA:83601Заболевание
Not applicable

Stevens-Johnson syndrome

ORPHA:36426Клин. подтип
Not applicable

Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum

ORPHA:95455Заболевание
Not applicable

Stickler syndrome

ORPHA:828Заболевание
Autosomal dominant, Autosomal recessive

Stickler syndrome type 1

ORPHA:90653Клин. подтип
Autosomal dominant

Stickler syndrome type 2

ORPHA:90654Клин. подтип
Autosomal dominant

Stiff person spectrum disorder

ORPHA:3198Заболевание
Not applicable

Stiff skin syndrome

ORPHA:2833Заболевание
Autosomal dominant

Stimmler syndrome

ORPHA:3199Мальформация
Autosomal recessive

Stormorken-Sjaastad-Langslet syndrome

ORPHA:3204Заболевание
Autosomal dominant

Streptobacillary rat-bite fever

ORPHA:99905Этиол. подтип

Streptococcal toxic-shock syndrome

ORPHA:99918Этиол. подтип
Not applicable

Streptococcus pneumoniae-associated hemolytic uremic syndrome

ORPHA:544493Клин. подтип

Striate palmoplantar keratoderma

ORPHA:50942Заболевание
Autosomal dominant