MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

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

ORPHA:231140Ätl. subt.
Not applicable, Unknown

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

ORPHA:231147Ätl. subt.
Not applicable, Unknown

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

ORPHA:96182Ätl. subt.

Simple cryoglobulinemia

ORPHA:91139Kr.

Simpson-Golabi-Behmel syndrome

ORPHA:373Malf.
X-linked recessive

Sinding-Larsen-Johansson disease

ORPHA:97337Kr.
Not applicable

Single-organ polyarteritis nodosa

ORPHA:439755Kl. subt.
Not applicable

Single-system multifocal Langerhans cell histiocytosis

ORPHA:687738Kl. subt.
Not applicable

Singleton-Merten dysplasia

ORPHA:85191Malf.
Autosomal dominant

Sinoatrial node dysfunction and deafness

ORPHA:324321Kr.
Autosomal recessive

Sirenomelia

ORPHA:3169Malf.
Not applicable

Sitosterolemia

ORPHA:2882Kr.
Autosomal recessive

Situs ambiguus

ORPHA:157769Morph.
Multigenic/multifactorial

Situs inversus totalis

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

Sjögren-Larsson syndrome

ORPHA:816Kr.
Autosomal recessive

Skeletal Ewing sarcoma

ORPHA:319Kr.
Not applicable

Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome

ORPHA:508533Kr.
Autosomal recessive

Skeletal dysplasia-epilepsy-short stature syndrome

ORPHA:1858Malf.

Skin fragility-woolly hair-palmoplantar keratoderma syndrome

ORPHA:293165Kr.
Autosomal dominant, Autosomal recessive

Sleep-related hypermotor epilepsy

ORPHA:98784Kr.
Autosomal dominant

Slow-channel congenital myasthenic syndrome

ORPHA:716765Ätl. subt.
Autosomal dominant, Autosomal recessive

Small bowel atresia

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

Small cell carcinoma of the bladder

ORPHA:284400Kr.
Not applicable

Small cell carcinoma of the ovary

ORPHA:370396Kr.
Not applicable