Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Alpha-mannosidosis, infantile form
Autosomal recessive
Infancy
Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3
Autosomal recessive
Adolescent, Childhood
Alpha-thalassemia
Autosomal recessive
All ages
Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
Not applicable, Unknown
Infancy, Neonatal
Alpha-thalassemia-myelodysplastic syndrome
Not applicable
Adult
Alport syndrome
Autosomal dominant, Autosomal recessive, X-linked dominant
Adolescent, Adult, Childhood, Elderly
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
X-linked recessive
Antenatal, Infancy, Neonatal
Alström syndrome
Autosomal recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Alternating hemiplegia of childhood
Autosomal dominant, Not applicable
Infancy, Neonatal
Alveolar echinococcosis
Not applicable
Adult, Elderly
Alveolar rhabdomyosarcoma
Multigenic/multifactorial
Alveolar soft tissue sarcoma
Not applicable
All ages
Amaurosis-hypertrichosis syndrome
Autosomal recessive
Neonatal
Amelo-onycho-hypohidrotic syndrome
No data available
Ameloblastic carcinoma
Not applicable
All ages
Ameloblastoma
Not applicable
All ages
Amelocerebrohypohidrotic syndrome
Autosomal recessive
Childhood, Infancy, Neonatal
Amelogenesis imperfecta
Autosomal dominant, Autosomal recessive, X-linked dominant
Infancy, Neonatal
American trypanosomiasis
Not applicable
All ages
Aminoacylase 1 deficiency
Autosomal recessive
Childhood
Aminopterin/methotrexate embryofetopathy
Not applicable
Antenatal, Neonatal
Amish lethal microcephaly
Autosomal recessive
Antenatal, Infancy, Neonatal
Amish nemaline myopathy
Autosomal recessive
Neonatal
Amniotic band syndrome
Antenatal, Neonatal