Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Multiple epiphyseal dysplasia type 5
Autosomal dominant
Childhood
Multiple epiphyseal dysplasia type 7
Childhood
Multiple epiphyseal dysplasia, Lowry type
Neonatal
Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome
Autosomal recessive
Infancy, Neonatal
Multiple epiphyseal dysplasia-miniepiphyses syndrome
Childhood, Infancy
Multiple epiphyseal dysplasia-severe proximal femoral dysplasia syndrome
Childhood
Multiple mitochondrial dysfunctions syndrome type 1
Autosomal recessive
Neonatal
Multiple mitochondrial dysfunctions syndrome type 2
Autosomal recessive
Neonatal
Multiple mitochondrial dysfunctions syndrome type 3
Autosomal recessive
Infancy, Neonatal
Multiple mitochondrial dysfunctions syndrome type 4
Autosomal recessive
Infancy
Multiple mitochondrial dysfunctions syndrome type 5
Autosomal recessive
Infancy
Multiple mitochondrial dysfunctions syndrome type 6
Autosomal recessive
Infancy
Multiple myeloma
Not applicable
Adult
Multiple osteochondromas
Autosomal dominant
Childhood
Multiple paragangliomas associated with polycythemia
Not applicable
Childhood
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
Unknown
Childhood
Multiple self-healing squamous epithelioma
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Multiple sulfatase deficiency
Autosomal recessive
Adolescent, Antenatal, Childhood, Infancy, Neonatal
Multiple symmetric lipomatosis
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, Not applicable
Adolescent, Adult, Childhood, Elderly
Multiple system atrophy
Multigenic/multifactorial, Not applicable
Adult
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