Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Moderate hemophilia B
X-linked recessive
Infancy, Neonatal
Moderate multiminicore disease with hand involvement
Autosomal dominant
Childhood, Infancy, Neonatal
Moderately-differentiated thymic neuroendocrine carcinoma
Not applicable
Adult
Moebius syndrome
Autosomal dominant
Antenatal, Neonatal
Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome
Not applicable
Infancy, Neonatal
Mohr-Tranebjaerg syndrome
X-linked recessive
Childhood
Monilethrix
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Monoamine oxidase A deficiency
X-linked recessive
Childhood
Monoclonal mast cell activation syndrome
All ages
Monomelic amyotrophy
Unknown
Adolescent, Adult
Mononen-Karnes-Senac syndrome
X-linked dominant
Infancy, Neonatal
Monosomy 13q14 syndrome
Not applicable
Infancy, Neonatal
Monosomy 13q34 syndrome
Not applicable
Antenatal, Neonatal
Monosomy 18p syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Monosomy 18q syndrome
Autosomal dominant
Antenatal, Neonatal
Monosomy 22 syndrome
Neonatal
Monosomy 5p syndrome
Not applicable, Unknown
Antenatal
Monosomy 9p syndrome
Antenatal, Neonatal
Monosomy 9q22.3 syndrome
Not applicable, Unknown
Infancy, Neonatal
Monosomy X syndrome
Not applicable
Antenatal, Childhood, Infancy, Neonatal
Monostotic fibrous dysplasia
Not applicable
Morgagni-Stewart-Morel syndrome
Autosomal dominant, X-linked recessive
Adult
Morning glory disc anomaly
Childhood
Morvan syndrome
Adult