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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Staphylococcal toxemia

ORPHA:300579Кат.

Staphylococcal toxic-shock syndrome

ORPHA:99919Этиол. подт.
Not applicable

Stargardt disease

ORPHA:827Заболевание
Autosomal dominant, Autosomal recessive

Steatocystoma multiplex-natal teeth syndrome

ORPHA:3184Порок
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.
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. подт.
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. подт.
Autosomal dominant

Stickler syndrome type 2

ORPHA:90654Клин. подт.
Autosomal dominant

Stiff person spectrum disorder

ORPHA:3198Заболевание
Not applicable

Stiff skin syndrome

ORPHA:2833Заболевание
Autosomal dominant

Stimmler syndrome

ORPHA:3199Порок
Autosomal recessive

Stormorken-Sjaastad-Langslet syndrome

ORPHA:3204Заболевание
Autosomal dominant

Streptobacillary rat-bite fever

ORPHA:99905Этиол. подт.

Streptococcal toxic-shock syndrome

ORPHA:99918Этиол. подт.
Not applicable

Streptococcus pneumoniae-associated hemolytic uremic syndrome

ORPHA:544493Клин. подт.

Striate palmoplantar keratoderma

ORPHA:50942Заболевание
Autosomal dominant