Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Mounier-Kühn syndrome
Not applicable
All ages
Mowat-Wilson syndrome
Autosomal dominant
Antenatal, Neonatal
Mowat-Wilson syndrome due to a ZEB2 point mutation
Autosomal dominant
Antenatal, Neonatal
Mowat-Wilson syndrome due to monosomy 2q22
Antenatal, Neonatal
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
Mu-heavy chain disease
Adult
Mucinous adenocarcinoma of ovary
Adult
Mucinous adenocarcinoma of the appendix
Adult, Elderly
Mucinous cystadenocarcinoma of the pancreas
Not applicable
Adult
Mucinous cystadenoma of childhood
Childhood
Mucinous tubular and spindle cell renal carcinoma
Adolescent, Adult, Elderly
Muckle-Wells syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
Mucocutaneous venous malformations
Autosomal dominant
All ages
Mucolipidosis type II
Autosomal recessive
Antenatal, Neonatal
Mucolipidosis type III
Autosomal recessive
Childhood
Mucolipidosis type III alpha/beta
Autosomal recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Mucolipidosis type III gamma
Autosomal recessive
Mucolipidosis type IV
Autosomal recessive
Infancy
Mucopolysaccharidosis
Mucopolysaccharidosis type 1
Autosomal recessive
All ages
Mucopolysaccharidosis type 10
Autosomal recessive
Childhood
Mucopolysaccharidosis type 2
X-linked recessive
Childhood