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Редкие (орфанные) заболевания
Полная база 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, препаратами и исследованиями.
7,547
Заболевания
4 552
Гены
8 700
Фенотипы
140
Регионы
Все (7,547)Bio anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformationMorphological anomalyClinical 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