MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

SLC40A1-related hemochromatosis

ORPHA:647834Disease
Autosomal dominant

SMARCA4-deficient sarcoma of thorax

ORPHA:466962Disease
Not applicable

SMPX-related distal myopathy

ORPHA:700163Disease
X-linked recessive

SPONASTRIME dysplasia

ORPHA:93357Disease
Autosomal recessive

SRD5A3-CDG

ORPHA:324737Disease
Autosomal recessive

SSR4-CDG

ORPHA:370927Disease
X-linked recessive

ST3GAL3-CDG

ORPHA:697734Disease
Autosomal recessive

STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome

ORPHA:391487Disease
Autosomal dominant

STAT3-related early-onset multisystem autoimmune disease

ORPHA:438159Disease
Autosomal dominant

STING-associated vasculopathy with onset in infancy

ORPHA:425120Disease
Autosomal dominant

STT3A-CDG

ORPHA:370921Disease
Autosomal recessive

STT3B-CDG

ORPHA:370924Disease
Autosomal recessive

STXBP1-related encephalopathy

ORPHA:599373Disease
Autosomal dominant

SUNCT syndrome

ORPHA:57145Disease
Not applicable

SURF1-related Charcot-Marie-Tooth disease type 4

ORPHA:391351Disease
Autosomal recessive

SYNGAP1-related developmental and epileptic encephalopathy

ORPHA:544254Disease
Autosomal dominant

Saccharopinuria

ORPHA:3124Disease
Autosomal recessive

Saldino-Mainzer syndrome

ORPHA:140969Disease
Autosomal recessive

Salivary gland type cancer of the breast

ORPHA:213557Disease

Sandhoff disease

ORPHA:796Disease
Autosomal recessive

Sandifer syndrome

ORPHA:71272Disease
Not applicable

Sarcocystosis

ORPHA:54368Disease

Sarcoidosis

ORPHA:797Disease
Multigenic/multifactorial

Sarcosinemia

ORPHA:3129Disease
Autosomal recessive