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

Multisystem Langerhans cell histiocytosis

ORPHA:687741Kl. subt.
Not applicable

Myelodysplastic neoplasm with increased blasts type 1

ORPHA:100019Kl. subt.
Not applicable

Myelodysplastic neoplasm with increased blasts type 2

ORPHA:100020Kl. subt.
Not applicable

Nasal encephalocele

ORPHA:141118Kl. subt.
Unknown

Necrotizing cellulitis

ORPHA:699678Kl. subt.
Not applicable

Necrotizing fasciitis

ORPHA:699697Kl. subt.
Not applicable

Necrotizing myositis

ORPHA:699702Kl. subt.
Not applicable

Neonatal glycine encephalopathy

ORPHA:289857Kl. subt.
Autosomal recessive

Neurogenic thoracic outlet syndrome

ORPHA:100073Kl. subt.
Not applicable

Niemann-Pick disease type C, adult neurologic onset

ORPHA:216986Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, juvenile neurologic onset

ORPHA:216981Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, late infantile neurologic onset

ORPHA:216978Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, severe early infantile neurologic onset

ORPHA:216975Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, severe perinatal form

ORPHA:216972Kl. subt.
Autosomal recessive

Nodular urticaria pigmentosa

ORPHA:158772Kl. subt.
Autosomal dominant, Unknown

Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325529Kl. subt.
Autosomal recessive

Non-fibrotic hypersensitivity pneumonitis

ORPHA:686462Kl. subt.
Not applicable

Non-hereditary retinoblastoma

ORPHA:357034Kl. subt.
Not applicable

Non-immune hydrops fetalis

ORPHA:363999Kl. subt.
Not applicable

Normosmic congenital hypogonadotropic hypogonadism

ORPHA:432Kl. subt.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive

Northern epilepsy

ORPHA:1947Kl. subt.
Autosomal recessive

Null syndrome

ORPHA:280234Kl. subt.
X-linked recessive

Occipital encephalocele

ORPHA:268823Kl. subt.
Autosomal dominant

Ocular cystinosis

ORPHA:411641Kl. subt.
Autosomal recessive