MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Staphylococcal toxemia

ORPHA:300579Kat.

Staphylococcal toxic-shock syndrome

ORPHA:99919Ätl. subt.
Not applicable

Stargardt disease

ORPHA:827Kr.
Autosomal dominant, Autosomal recessive

Steatocystoma multiplex-natal teeth syndrome

ORPHA:3184Malf.
Autosomal dominant

Steel syndrome

ORPHA:438117Kr.
Autosomal recessive

Steinert myotonic dystrophy

ORPHA:273Kr.
Autosomal dominant

Stellate multiform amelanotic choroidopathy

ORPHA:674958Kr.

Sterile multifocal osteomyelitis with periostitis and pustulosis

ORPHA:210115Kr.
Autosomal recessive

Sternal cleft

ORPHA:2017Morph.
Not applicable

Steroid dehydrogenase deficiency-dental anomalies syndrome

ORPHA:3196Kr.
Autosomal recessive

Steroid-responsive encephalopathy associated with autoimmune thyroiditis

ORPHA:83601Kr.
Not applicable

Stevens-Johnson syndrome

ORPHA:36426Kl. subt.
Not applicable

Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum

ORPHA:95455Kr.
Not applicable

Stickler syndrome

ORPHA:828Kr.
Autosomal dominant, Autosomal recessive

Stickler syndrome type 1

ORPHA:90653Kl. subt.
Autosomal dominant

Stickler syndrome type 2

ORPHA:90654Kl. subt.
Autosomal dominant

Stiff person spectrum disorder

ORPHA:3198Kr.
Not applicable

Stiff skin syndrome

ORPHA:2833Kr.
Autosomal dominant

Stimmler syndrome

ORPHA:3199Malf.
Autosomal recessive

Stormorken-Sjaastad-Langslet syndrome

ORPHA:3204Kr.
Autosomal dominant

Streptobacillary rat-bite fever

ORPHA:99905Ätl. subt.

Streptococcal toxic-shock syndrome

ORPHA:99918Ätl. subt.
Not applicable

Streptococcus pneumoniae-associated hemolytic uremic syndrome

ORPHA:544493Kl. subt.

Striate palmoplantar keratoderma

ORPHA:50942Kr.
Autosomal dominant