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

Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome

ORPHA:293987Kr.
Unknown

Rapid-onset dystonia-parkinsonism

ORPHA:71517Kr.
Autosomal dominant, Not applicable

Rapidly involuting congenital hemangioma

ORPHA:141184Kr.
Not applicable

Rare adenocarcinoma of the breast

ORPHA:213528Kr.

Rare isolated myopia

ORPHA:98619Kr.
Autosomal dominant, Autosomal recessive

Rare non-syndromic genetic deafness

ORPHA:87884Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Rare non-syndromic intellectual disability

ORPHA:101685Kr.
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Rasmussen subacute encephalitis

ORPHA:1929Kr.
Not applicable

Rat-bite fever

ORPHA:31205Kr.

Ravine syndrome

ORPHA:99852Kr.
Autosomal recessive

Reactive arthritis

ORPHA:29207Kr.
Multigenic/multifactorial, Not applicable

Recessive X-linked ichthyosis

ORPHA:461Kr.
X-linked recessive

Recessive dystrophic epidermolysis bullosa inversa

ORPHA:79409Kr.
Autosomal recessive

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

ORPHA:280384Kr.
Autosomal recessive

Recessive mitochondrial ataxia syndrome

ORPHA:94125Kr.
Autosomal recessive

Recurrent Neisseria infections due to factor D deficiency

ORPHA:169467Kr.
Autosomal recessive

Recurrent infections associated with rare immunoglobulin isotypes deficiency

ORPHA:183675Kr.
Unknown

Recurrent infections due to specific granule deficiency

ORPHA:169142Kr.
Autosomal recessive

Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome

ORPHA:480864Kr.
Autosomal recessive

Recurrent respiratory papillomatosis

ORPHA:60032Kr.
Not applicable

Reducing body myopathy

ORPHA:97239Kr.
Not applicable, X-linked dominant

Refractory anemia with excess blasts in transformation

ORPHA:168960Kr.

Refractory celiac disease

ORPHA:398063Kr.
Not applicable

Regional odontodysplasia

ORPHA:83450Kr.
Not applicable