Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Moebius syndrome
Autosomal dominant
Antenatal, 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
Monosomy 18p syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Morvan syndrome
Adult
Mosaic NF2-related schwannomatosis
Infancy, Neonatal
Mosaic neurofibromatosis type 1
Infancy, Neonatal
Mosaic schwannomatosis
Infancy, Neonatal
Motor incoordination-myopathy-respiratory insufficiency-progressive cerebellar atrophy syndrome
Autosomal recessive
Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
X-linked recessive
All ages
Moyamoya disease
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive
All ages
Moyamoya disease with early-onset achalasia
Autosomal recessive
Infancy, Neonatal
Mucinous adenocarcinoma of ovary
Adult
Mucinous adenocarcinoma of the appendix
Adult, Elderly
Mucinous cystadenocarcinoma of the pancreas
Not applicable
Adult
Mucinous tubular and spindle cell renal carcinoma
Adolescent, Adult, Elderly
Muckle-Wells syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
Mucolipidosis type II
Autosomal recessive
Antenatal, Neonatal
Mucolipidosis type III
Autosomal recessive
Childhood
Mucolipidosis type IV
Autosomal recessive
Infancy
Mucopolysaccharidosis type 1
Autosomal recessive
All ages