Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Native American myopathy
Autosomal recessive
Infancy, Neonatal
Navajo neurohepatopathy
Autosomal recessive
Childhood, Infancy
Naxos disease
Autosomal recessive
Infancy, Neonatal
Necrobiosis lipoidica
Adolescent, Adult, Childhood, Elderly
Necrobiotic xanthogranuloma
Not applicable
Necrotizing cellulitis
Not applicable
Necrotizing enterocolitis
Not applicable
Neonatal
Necrotizing fasciitis
Not applicable
Necrotizing myositis
Not applicable
Necrotizing soft tissue infection
Not applicable
All ages
Nelson syndrome
Adult, Elderly
Nemaline myopathy
Autosomal dominant, Autosomal recessive, Not applicable
All ages
Neonatal Marfan syndrome
Autosomal dominant
Infancy, Neonatal
Neonatal acute respiratory distress syndrome
Autosomal recessive
Neonatal
Neonatal adrenoleukodystrophy
Autosomal recessive
Childhood, Infancy, Neonatal
Neonatal alloimmune neutropenia
Neonatal
Neonatal antiphospholipid syndrome
Neonatal
Neonatal autoimmune hemolytic anemia
Neonatal
Neonatal compartment syndrome
Neonatal
Neonatal dermatomyositis
Neonatal
Neonatal diabetes mellitus
Autosomal dominant, Autosomal recessive, Not applicable
Infancy, Neonatal
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome
Autosomal recessive
Neonatal
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Neonatal epileptic encephalopathy due to glutaminase deficiency
Autosomal recessive
Neonatal