Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Mucopolysaccharidosis type 10
Autosomal recessive
Childhood
Mucopolysaccharidosis type 2
X-linked recessive
Childhood
Mucopolysaccharidosis type 3
Autosomal recessive
Childhood
Mucopolysaccharidosis type 4
Autosomal recessive
Childhood, Infancy
Mucopolysaccharidosis type 6
Autosomal recessive
Childhood
Mucopolysaccharidosis type 7
Autosomal recessive
Adolescent, Antenatal, Childhood, Infancy, Neonatal
Mucous membrane pemphigoid
Not applicable
Adolescent, Adult, Childhood, Elderly, Infancy
Mueller-Weiss syndrome
Adult
Multicentric osteolysis-nodulosis-arthropathy spectrum
Autosomal recessive
Childhood, Infancy
Multicentric reticulohistiocytosis
Not applicable
Adult
Multifocal atrial tachycardia
Not applicable
Infancy, Neonatal
Multifocal infantile hemangioma with extracutenous involvement
Not applicable
Neonatal
Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
Not applicable
Infancy, Neonatal
Multifocal motor neuropathy
Unknown
Adult
Multifocal pattern dystrophy simulating fundus flavimaculatus
Autosomal dominant
Adult
Multiminicore myopathy
Autosomal dominant, Autosomal recessive
Antenatal, Childhood, Infancy, Neonatal
Multiple acyl-CoA dehydrogenase deficiency
Autosomal recessive
All ages
Multiple benign circumferential skin creases on limbs
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Multiple endocrine neoplasia type 1
Autosomal dominant, Not applicable
All ages
Multiple endocrine neoplasia type 2
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Multiple endocrine neoplasia type 4
Autosomal dominant, Not applicable
Adult
Multiple epiphyseal dysplasia due to collagen 9 anomaly
Autosomal dominant
Adolescent, Childhood
Multiple epiphyseal dysplasia type 1
Autosomal dominant
Childhood
Multiple epiphyseal dysplasia type 4
Autosomal recessive
Childhood