Orphanet Database • Orphadata CC-BY-4.0
Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
7,547
Заболеваний
4 552
Генов
8 700
Фенотипов
140
Регионов
Все (7,547)Biological anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformation syndromeMorphological anomalyParticular clinical situation in a disease or syndrome
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