MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Squamous cell carcinoma of the rectum

ORPHA:424002Kr.
Not applicable

Squamous cell carcinoma of the small intestine

ORPHA:423968Kr.
Not applicable

Squamous cell carcinoma of the stomach

ORPHA:418959Kr.
Not applicable

St. Louis encephalitis

ORPHA:83484Kr.
Not applicable

Staphylococcal necrotizing pneumonia

ORPHA:36238Kr.
Not applicable

Staphylococcal scalded skin syndrome

ORPHA:36236Kr.

Staphylococcal scarlet fever

ORPHA:36235Kr.

Stargardt disease

ORPHA:827Kr.
Autosomal dominant, Autosomal recessive

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

Steroid dehydrogenase deficiency-dental anomalies syndrome

ORPHA:3196Kr.
Autosomal recessive

Steroid-responsive encephalopathy associated with autoimmune thyroiditis

ORPHA:83601Kr.
Not applicable

Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum

ORPHA:95455Kr.
Not applicable

Stickler syndrome

ORPHA:828Kr.
Autosomal dominant, Autosomal recessive

Stiff person spectrum disorder

ORPHA:3198Kr.
Not applicable

Stiff skin syndrome

ORPHA:2833Kr.
Autosomal dominant

Stormorken-Sjaastad-Langslet syndrome

ORPHA:3204Kr.
Autosomal dominant

Striate palmoplantar keratoderma

ORPHA:50942Kr.
Autosomal dominant

Strongyloidiasis

ORPHA:76Kr.
Not applicable

Subacute cutaneous lupus erythematosus

ORPHA:163525Kr.

Subacute inflammatory demyelinating polyneuropathy

ORPHA:206594Kr.

Subacute sclerosing leukoencephalitis

ORPHA:2806Kr.
Not applicable