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

Short stature-delayed bone age due to thyroid hormone metabolism deficiency

ORPHA:171706Kr.
Autosomal recessive

Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome

ORPHA:314394Kr.
Autosomal recessive

Short stature-pituitary and cerebellar defects-small sella turcica syndrome

ORPHA:85442Kr.
Autosomal dominant

Short-limb skeletal dysplasia with severe combined immunodeficiency

ORPHA:935Kr.
Not applicable

Shwachman-Diamond syndrome

ORPHA:811Kr.
Autosomal recessive

Sialidosis type 1

ORPHA:812Kr.
Autosomal recessive

Sialidosis type 2

ORPHA:87876Kr.
Autosomal recessive

Sialuria

ORPHA:3166Kr.
Autosomal dominant

Sickle cell S-C disease

ORPHA:251365Kr.
Autosomal recessive

Sickle cell anemia

ORPHA:232Kr.
Autosomal recessive

Sickle cell-beta-thalassemia disease

ORPHA:251359Kr.
Autosomal recessive

Silent sinus syndrome

ORPHA:71276Kr.
Not applicable

Silver-Russell syndrome

ORPHA:813Kr.
Autosomal dominant, Not applicable

Simple cryoglobulinemia

ORPHA:91139Kr.

Sinding-Larsen-Johansson disease

ORPHA:97337Kr.
Not applicable

Sinoatrial node dysfunction and deafness

ORPHA:324321Kr.
Autosomal recessive

Sitosterolemia

ORPHA:2882Kr.
Autosomal recessive

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

Skin fragility-woolly hair-palmoplantar keratoderma syndrome

ORPHA:293165Kr.
Autosomal dominant, Autosomal recessive

Sleep-related hypermotor epilepsy

ORPHA:98784Kr.
Autosomal dominant

Small cell carcinoma of the bladder

ORPHA:284400Kr.
Not applicable

Small cell carcinoma of the ovary

ORPHA:370396Kr.
Not applicable