Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Large granular lymphocyte leukemia
Lateral facial cleft
Antenatal, Neonatal
Lichen myxedematosus
Adult, Infancy
Limb-girdle muscular dystrophy
Autosomal dominant, Autosomal recessive
All ages
Lissencephaly with cerebellar hypoplasia
Localized lipodystrophy
Unknown
All ages
Marginal papular palmoplantar keratoderma
Autosomal dominant
Marginal zone lymphoma
Adult
Median facial cleft
Antenatal, Neonatal
Mendelian susceptibility to mycobacterial diseases
Autosomal dominant, Autosomal recessive, X-linked recessive
All ages
Methylmalonic acidemia without homocystinuria
Autosomal dominant, Autosomal recessive, X-linked dominant
All ages
Mitochondrial DNA depletion syndrome, encephalomyopathic form
Autosomal recessive
Infancy, Neonatal
Mitochondrial DNA depletion syndrome, hepatocerebral form
Autosomal recessive
Infancy, Neonatal
Mitochondrial DNA-related mitochondrial myopathy
Mitochondrial inheritance
Multiple carboxylase deficiency
Autosomal recessive
Infancy, Neonatal
Multiple endocrine neoplasia
Autosomal dominant, Not applicable
All ages
Multiple epiphyseal dysplasia
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Multiple mitochondrial dysfunctions syndrome
Autosomal recessive
Mycosis fungoides and variants
Not applicable
Adult
Myelocystocele
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Myelodysplastic syndrome
All ages
Myelodysplastic/myeloproliferative disease
Myeloproliferative neoplasm
All ages