Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Myelodysplastic syndrome
All ages
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Not applicable
Adult
Myelodysplastic/myeloproliferative disease
Myeloid sarcoma
Not applicable
All ages
Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement
Myeloid/lymphoid neoplasm associated with JAK2 rearrangement
Adolescent, Adult, Childhood, Elderly
Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement
Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement
Myeloperoxidase deficiency
Autosomal recessive
All ages
Myeloproliferative neoplasm
All ages
Myhre syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Myoclonic epilepsy in non-progressive encephalopathies
Childhood, Infancy
Myoclonic epilepsy of infancy
Autosomal recessive
Infancy
Myoclonus-cerebellar ataxia-deafness syndrome
Autosomal dominant
Childhood
Myoclonus-dystonia syndrome
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood
Myofibrillar myopathy
Autosomal dominant, Autosomal recessive
Adult
Myopathic Ehlers-Danlos syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Infancy, Neonatal
Myopathic intestinal pseudoobstruction
Unknown
Myopathy and diabetes mellitus
Mitochondrial inheritance
Adolescent, Adult, Childhood, Infancy, Neonatal
Myosclerosis
Autosomal recessive
Childhood
Myosin storage myopathy
Autosomal dominant, Autosomal recessive
Myospherulosis
Not applicable
Adult
Myotonia fluctuans
Autosomal dominant
Childhood
Myotonia permanens
Autosomal dominant
Childhood