Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Macrodactyly of toes, unilateral
Autosomal dominant
Macrophage activation syndrome
Adolescent, Adult, Childhood
Macrophagic myofasciitis
Not applicable
Adolescent, Adult, Childhood, Elderly
Macrosomia-microphthalmia-cleft palate syndrome
Antenatal, Neonatal
Macrostomia-preauricular tags-external ophthalmoplegia syndrome
Autosomal dominant
Infancy, Neonatal
Macrothrombocytopenia with mitral valve insufficiency
Childhood
Macular coloboma-cleft palate-hallux valgus syndrome
Autosomal recessive
Neonatal
Macular corneal dystrophy
Autosomal recessive
All ages
Maculopapular cutaneous mastocytosis
Not applicable
All ages
Madras motor neuron disease
Not applicable, X-linked recessive
Adolescent, Adult, Childhood
Maffucci syndrome
Not applicable
Childhood
Majeed syndrome
Autosomal recessive
Childhood, Infancy
Mal de Meleda
Autosomal recessive
Childhood, Infancy
Mal de débarquement
Not applicable
All ages
Malakoplakia
Unknown
Adult
Malan overgrowth syndrome
Autosomal dominant, Unknown
Infancy
Malaria
Not applicable
All ages
Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome
Unknown
Neonatal
Male infertility due to acephalic spermatozoa
Autosomal recessive
Adult
Male infertility due to globozoospermia
Autosomal recessive
Adult
Male infertility due to large-headed multiflagellar polyploid spermatozoa
Autosomal recessive
Male infertility with azoospermia or oligozoospermia due to single gene mutation
Autosomal dominant, Autosomal recessive, X-linked recessive
Adolescent, Adult
Male infertility with teratozoospermia due to single gene mutation
Adolescent, Adult