MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
727 Erkrankungen gefunden (Kl. subt.) Zurücksetzen

Acute endophthalmitis

ORPHA:279888Kl. subt.
Not applicable

Acute mast cell leukemia

ORPHA:566393Kl. subt.
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Kl. subt.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Kl. subt.
Not applicable

Acute neonatal citrullinemia type I

ORPHA:247546Kl. subt.
Autosomal recessive

Acute transverse myelitis with anti-MOG antibodies

ORPHA:592873Kl. subt.

Adrenomyeloneuropathy

ORPHA:139399Kl. subt.
X-linked recessive

Adult CLN1 disease

ORPHA:699745Kl. subt.
Autosomal recessive

Adult CLN5 disease

ORPHA:699812Kl. subt.
Autosomal recessive

Adult CLN6 disease

ORPHA:700477Kl. subt.
Autosomal recessive

Adult Krabbe disease

ORPHA:206448Kl. subt.
Autosomal recessive

Adult hypophosphatasia

ORPHA:247676Kl. subt.
Autosomal dominant, Autosomal recessive

Adult intestinal botulism

ORPHA:178487Kl. subt.

Adult polyglucosan body disease

ORPHA:206583Kl. subt.
Autosomal recessive

Adult-onset Steinert myotonic dystrophy

ORPHA:589830Kl. subt.
Autosomal dominant

Adult-onset myasthenia gravis

ORPHA:391490Kl. subt.
Multigenic/multifactorial, Not applicable

Alexander disease type I

ORPHA:363717Kl. subt.
Not applicable

Alexander disease type II

ORPHA:363722Kl. subt.
Autosomal dominant

Alobar holoprosencephaly

ORPHA:93925Kl. subt.
Multigenic/multifactorial, Not applicable

Alpha-N-acetylgalactosaminidase deficiency type 1

ORPHA:79279Kl. subt.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 2

ORPHA:79280Kl. subt.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 3

ORPHA:79281Kl. subt.
Autosomal recessive

Alpha-heavy chain disease

ORPHA:100025Kl. subt.

Alpha-mannosidosis, adult form

ORPHA:309288Kl. subt.
Autosomal recessive