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

Cone rod dystrophy-short stature syndrome

ORPHA:653709Kr.
Autosomal recessive

Confetti-like macular atrophy

ORPHA:221142Kr.

Congenital Epstein-Barr virus infection

ORPHA:70596Kr.
Not applicable

Congenital abducens nerve palsy

ORPHA:440233Kr.
Not applicable

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ORPHA:90795Kr.
Autosomal recessive

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

ORPHA:90793Kr.
Autosomal recessive

Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency

ORPHA:90791Kr.
Autosomal recessive

Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency

ORPHA:95699Kr.
Autosomal recessive

Congenital alpha2-antiplasmin deficiency

ORPHA:79Kr.
Autosomal recessive

Congenital alveolar capillary dysplasia

ORPHA:210122Kr.
Autosomal dominant

Congenital amegakaryocytic thrombocytopenia

ORPHA:3319Kr.
Autosomal recessive

Congenital analbuminemia

ORPHA:86816Kr.
Autosomal recessive

Congenital atransferrinemia

ORPHA:1195Kr.
Autosomal recessive

Congenital autosomal recessive small-platelet thrombocytopenia

ORPHA:566192Kr.
Autosomal recessive

Congenital axonal neuropathy with encephalopathy

ORPHA:538101Kr.

Congenital bile acid synthesis defect type 1

ORPHA:79301Kr.
Autosomal recessive

Congenital bile acid synthesis defect type 2

ORPHA:79303Kr.
Autosomal recessive

Congenital bile acid synthesis defect type 3

ORPHA:79302Kr.
Autosomal recessive

Congenital bile acid synthesis defect type 4

ORPHA:79095Kr.
Autosomal recessive

Congenital brain dysgenesis due to glutamine synthetase deficiency

ORPHA:71278Kr.
Autosomal recessive

Congenital cataract-hearing loss-severe developmental delay syndrome

ORPHA:300313Kr.
Autosomal recessive

Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome

ORPHA:1369Kr.
Autosomal recessive

Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome

ORPHA:330054Kr.
Autosomal recessive

Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome

ORPHA:521432Kr.
Autosomal recessive