Orphanet Datenbank · Orphadata CC-BY-4.0
Seltene Erkrankungen (Orphan)
Komplette Bibliothek mit 7,547 Erkrankungen — Genetik, Phänotypen, Epidemiologie, Orphan-Arzneimittel und Studien.
7,547
Erkrankungen
4 552
Gene
8 700
Phänotypen
140
Regionen
Alle (7,547)Bio-AnomalieKategorieKlinische GruppeKlinischer SubtypClinical syndromeErkrankungÄtiologischer SubtypHistopathologischer SubtypMalformationssyndromMorphologische AnomalieBesondere klinische Situation
Beta-mercaptolactate cysteine disulfiduria
No data available
Carnosinase deficiency
Autosomal recessive
Infancy
Congenital deficiency in alpha-fetoprotein
Autosomal recessive
Antenatal, Neonatal
Familial Hyperalphalipoproteinemia
Autosomal dominant
Genetic hyperferritinemia without iron overload
Autosomal dominant, Autosomal recessive
No data available
Hereditary persistence of alpha-fetoprotein
Autosomal dominant
Adolescent
Idiopathic CD4 lymphocytopenia
Not applicable
Adult
Isolated asymptomatic elevation of creatine phosphokinase
Autosomal dominant
All ages
L-ferritin deficiency
Autosomal dominant, Autosomal recessive
Childhood
Lipoyl transferase 2 deficiency
No data available
No data available
Methylmalonic aciduria due to transcobalamin receptor defect
Autosomal recessive
Infancy, Neonatal