Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Matthew-Wood syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Maxillonasal dysplasia
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial
Neonatal
May-Thurner syndrome
Not applicable
Mayer-Rokitansky-Küster-Hauser syndrome
Autosomal dominant, Not applicable
Adolescent, Antenatal
Mayer-Rokitansky-Küster-Hauser syndrome type 1
Autosomal dominant, Not applicable
Adolescent, Antenatal
Mayer-Rokitansky-Küster-Hauser syndrome type 2
Autosomal dominant, Not applicable
Adolescent, Antenatal, Neonatal
Mazabraud syndrome
Not applicable
Adult
McCune-Albright syndrome
Not applicable
Childhood
McDonough syndrome
Infancy, Neonatal
McKusick-Kaufman syndrome
Autosomal recessive
Antenatal, Neonatal
McLeod neuroacanthocytosis syndrome
X-linked recessive
Adult
Meacham syndrome
Autosomal dominant
Infancy, Neonatal
Meckel syndrome
Autosomal recessive
Antenatal
Meconium aspiration syndrome
Not applicable
Infancy, Neonatal
Medial condensing osteitis of the clavicle
Not applicable
Adolescent, Adult, Childhood
Median cleft lip/mandible
Not applicable
Neonatal
Median facial cleft
Antenatal, Neonatal
Median nodule of the upper lip
Autosomal dominant
Infancy, Neonatal
Mediastinal arteriovenous malformation
Not applicable
Medich giant platelet syndrome
Infancy, Neonatal
Medium chain acyl-CoA dehydrogenase deficiency
Autosomal recessive
Infancy, Neonatal
Medullary sponge kidney
Autosomal dominant, Not applicable
Adult, Childhood
Medullary thyroid carcinoma
Not applicable
Adult
Medulloblastoma
Not applicable
All ages