MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Silver-Russell syndrome due to an imprinting defect of 11p15

ORPHA:231140Etio. sub.
Not applicable, Unknown

Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11

ORPHA:231147Etio. sub.
Not applicable, Unknown

Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7

ORPHA:96182Etio. sub.

Simple cryoglobulinemia

ORPHA:91139Disease

Simpson-Golabi-Behmel syndrome

ORPHA:373Malform.
X-linked recessive

Sinding-Larsen-Johansson disease

ORPHA:97337Disease
Not applicable

Single-organ polyarteritis nodosa

ORPHA:439755Clin. sub.
Not applicable

Single-system multifocal Langerhans cell histiocytosis

ORPHA:687738Clin. sub.
Not applicable

Singleton-Merten dysplasia

ORPHA:85191Malform.
Autosomal dominant

Sinoatrial node dysfunction and deafness

ORPHA:324321Disease
Autosomal recessive

Sirenomelia

ORPHA:3169Malform.
Not applicable

Sitosterolemia

ORPHA:2882Disease
Autosomal recessive

Situs ambiguus

ORPHA:157769Morph.
Multigenic/multifactorial

Situs inversus totalis

ORPHA:101063Morph.
Autosomal dominant, Autosomal recessive, Not applicable

Sjögren-Larsson syndrome

ORPHA:816Disease
Autosomal recessive

Skeletal Ewing sarcoma

ORPHA:319Disease
Not applicable

Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome

ORPHA:508533Disease
Autosomal recessive

Skeletal dysplasia-epilepsy-short stature syndrome

ORPHA:1858Malform.

Skin fragility-woolly hair-palmoplantar keratoderma syndrome

ORPHA:293165Disease
Autosomal dominant, Autosomal recessive

Sleep-related hypermotor epilepsy

ORPHA:98784Disease
Autosomal dominant

Slow-channel congenital myasthenic syndrome

ORPHA:716765Etio. sub.
Autosomal dominant, Autosomal recessive

Small bowel atresia

ORPHA:1201Morph.
Autosomal recessive, Not applicable, Unknown

Small cell carcinoma of the bladder

ORPHA:284400Disease
Not applicable

Small cell carcinoma of the ovary

ORPHA:370396Disease
Not applicable