Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Multisystem Langerhans cell histiocytosis
Not applicable
Multisystem inflammatory syndrome in children and adults
Childhood
Multisystemic smooth muscle dysfunction syndrome
Unknown
Infancy
Murine typhus
Not applicable
All ages
Muscle filaminopathy
Autosomal dominant
Adult
Muscle-eye-brain disease
Autosomal recessive
Antenatal, Infancy, Neonatal
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
Autosomal recessive
Infancy
Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
Autosomal dominant
Childhood
Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
Autosomal dominant
Infancy, Neonatal
Muscular pseudohypertrophy-hypothyroidism syndrome
Childhood
Musculocontractural Ehlers-Danlos syndrome
Autosomal recessive
Infancy, Neonatal
Mutilating hereditary sensory neuropathy with spastic paraplegia
Autosomal recessive
Childhood, Infancy
Mutilating palmoplantar keratoderma with periorificial keratotic plaques
Autosomal dominant, Not applicable, X-linked recessive
Childhood, Infancy, Neonatal
Myalgia-eosinophilia syndrome associated with tryptophan
Not applicable
All ages
Myasthenia gravis
Multigenic/multifactorial, Not applicable
All ages
Mycetoma
Not applicable
All ages
Mycophenolate mofetil embryopathy
Not applicable
Antenatal, Infancy, Neonatal
Mycoplasma encephalitis
Not applicable
All ages
Mycosis fungoides and variants
Not applicable
Adult
Myelocystocele
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Myelodysplastic neoplasm with increased blasts
Not applicable
Adult
Myelodysplastic neoplasm with increased blasts type 1
Not applicable
Adult
Myelodysplastic neoplasm with increased blasts type 2
Not applicable
Adult
Myelodysplastic neoplasm with low blasts
Not applicable
Adolescent, Adult, Childhood, Elderly, Infancy