Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Neuronal intranuclear inclusion disease
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Neurooculocardiogenitourinary syndrome
Autosomal dominant
Infancy, Neonatal
Neuropathy with hearing impairment
Autosomal dominant
Adult
Neurotrophic keratopathy
Not applicable
Adult, Childhood
Neurovascular malformation
All ages
Neutral lipid storage disease
Autosomal recessive
Infancy, Neonatal
Neutral lipid storage disease with ichthyosis
Autosomal recessive
Infancy, Neonatal
Neutral lipid storage disease with myopathy
Autosomal recessive
Adult
Neutropenia-monocytopenia-deafness syndrome
Unknown
Infancy, Neonatal
Nevus comedonicus syndrome
Not applicable
Childhood, Infancy, Neonatal
Nevus of Ito
Not applicable
All ages
Nevus of Ota
Not applicable
All ages
New-onset refractory status epilepticus
Adult
Nicolaides-Baraitser syndrome
Autosomal dominant
Infancy, Neonatal
Nicolau syndrome
Niemann-Pick disease type C
Autosomal recessive
All ages
Niemann-Pick disease type C, adult neurologic onset
Autosomal recessive
Adult
Niemann-Pick disease type C, juvenile neurologic onset
Autosomal recessive
Adolescent
Niemann-Pick disease type C, late infantile neurologic onset
Autosomal recessive
Childhood
Niemann-Pick disease type C, severe early infantile neurologic onset
Autosomal recessive
Infancy, Neonatal
Niemann-Pick disease type C, severe perinatal form
Autosomal recessive
Antenatal, Neonatal
Night blindness-skeletal anomalies-dysmorphism syndrome
Childhood
Nijmegen breakage syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Nijmegen breakage syndrome-like disorder
Autosomal recessive
Neonatal