Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Late-onset nephronophthisis
Autosomal recessive
Late-onset retinal degeneration
Autosomal dominant
Adult, Elderly
Lateral facial cleft
Antenatal, Neonatal
Lateral meningocele syndrome
Autosomal dominant
Infancy, Neonatal
Lathosterolosis
Autosomal recessive
Neonatal
Lattice corneal dystrophy type I
Autosomal dominant
All ages
Laubry-Pezzi syndrome
Infancy, Neonatal
Laurence-Moon syndrome
Autosomal recessive
Neonatal
Laurin-Sandrow syndrome
Autosomal dominant
Antenatal, Neonatal
Lead poisoning
Not applicable
All ages
Leber congenital amaurosis
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Leber hereditary optic neuropathy
Mitochondrial inheritance
Adolescent, Adult
Leber plus disease
Mitochondrial inheritance
Adolescent, Adult, Childhood, Infancy
Ledderhose disease
Adult
Left ventricular noncompaction
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, X-linked recessive
All ages
Legg-Calvé-Perthes disease
Autosomal dominant, Multigenic/multifactorial
Childhood
Legionnaires disease
Not applicable
All ages
Legius syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
Leigh syndrome
Autosomal recessive, Mitochondrial inheritance, X-linked recessive
All ages
Leiomyosarcoma
Not applicable
Adolescent, Adult, Childhood, Elderly
Leiomyosarcoma of the cervix uteri
Adult, Elderly
Leishmaniasis
Not applicable
All ages
Lelis syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Lemierre syndrome
Adolescent