MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Non-syndromic pontocerebellar hypoplasia

ORPHA:98523Clin. grp.
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:648Malform.
Autosomal dominant, Autosomal recessive

Noonan syndrome with multiple lentigines

ORPHA:500Malform.
Autosomal dominant

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

ORPHA:363972Malform.
Autosomal dominant

Noonan syndrome-like disorder with loose anagen hair

ORPHA:2701Malform.
Autosomal dominant

Normosmic congenital hypogonadotropic hypogonadism

ORPHA:432Clin. sub.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive

Norrie disease

ORPHA:649Malform.
X-linked recessive

North Carolina macular dystrophy

ORPHA:75327Disease
Autosomal dominant

Northern epilepsy

ORPHA:1947Clin. sub.
Autosomal recessive

Null pituitary adenoma

ORPHA:314790Hist. sub.
Not applicable