MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Non-syndromic pontocerebellar hypoplasia

ORPHA:98523Kl. gruppe
Autosomal recessive

Non-syndromic posterior hypospadias

ORPHA:95706Morph.
Multigenic/multifactorial, X-linked recessive

Non-syndromic pouch colon

ORPHA:601013Morph.

Non-syndromic rectal atresia

ORPHA:601018Morph.

Non-syndromic rectal stenosis

ORPHA:601023Morph.

Non-syndromic rectourethral fistula

ORPHA:600961Morph.

Non-syndromic rectovaginal fistula

ORPHA:601028Morph.

Non-syndromic rectovesical fistula

ORPHA:600984Morph.

Non-syndromic sagittal craniosynostosis

ORPHA:35093Morph.
Autosomal dominant, Not applicable

Non-syndromic unicoronal and sagittal craniosynostosis

ORPHA:620186Morph.

Non-syndromic unicoronal craniosynostosis

ORPHA:620102Morph.

Non-syndromic unifrontosphenoidal craniosynostosis

ORPHA:620139Morph.

Non-syndromic unilambdoid craniosynostosis

ORPHA:620113Morph.

Non-syndromic unisquamosal craniosynostosis

ORPHA:620146Morph.

Non-syndromic vestibular fistula

ORPHA:600993Morph.

Noonan syndrome

ORPHA:648Malf.
Autosomal dominant, Autosomal recessive

Noonan syndrome with multiple lentigines

ORPHA:500Malf.
Autosomal dominant

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

ORPHA:363972Malf.
Autosomal dominant

Noonan syndrome-like disorder with loose anagen hair

ORPHA:2701Malf.
Autosomal dominant

Normosmic congenital hypogonadotropic hypogonadism

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

Norrie disease

ORPHA:649Malf.
X-linked recessive

North Carolina macular dystrophy

ORPHA:75327Kr.
Autosomal dominant

Northern epilepsy

ORPHA:1947Kl. subt.
Autosomal recessive

Null pituitary adenoma

ORPHA:314790His. subt.
Not applicable