Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
NLRP3-associated autoinflammatory disease
Autosomal dominant, Not applicable
Adolescent, Childhood, Infancy, Neonatal
NMDA receptor encephalitis
Not applicable
All ages
NOCARH syndrome
Autosomal dominant
Infancy, Neonatal
NPHP3-related Meckel-like syndrome
Autosomal recessive
Childhood
NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance
Autosomal recessive
Neonatal
NTHL1-related polyposis
Autosomal recessive
Adult, Elderly
NUT midline carcinoma
Not applicable
Adolescent, Adult, Childhood, Elderly
Naegeli-Franceschetti-Jadassohn syndrome
Autosomal dominant
Infancy, Neonatal
Nager syndrome
Autosomal dominant, Autosomal recessive, Not applicable
Antenatal, Neonatal
Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
Autosomal recessive
Infancy
Nail-patella syndrome
Autosomal dominant
Antenatal, Childhood, Infancy, Neonatal
Nail-patella-like renal disease
Autosomal dominant
Infancy, Neonatal
Nance-Horan syndrome
X-linked dominant
Neonatal
Nanophthalmos
Autosomal dominant, Autosomal recessive, Not applicable
Infancy, Neonatal
Narcolepsy type 1
Unknown
Adolescent, Adult, Childhood
Narcolepsy type 2
Unknown
Adolescent, Adult, Childhood
Nasal encephalocele
Unknown
Nasal ganglioglioma
Antenatal, Neonatal
Nasal glial heterotopia
Not applicable
Nasolacrimal duct cyst
Not applicable
Adult, Infancy, Neonatal
Nasopalpebral lipoma-coloboma syndrome
Autosomal dominant
Neonatal
Nasopharyngeal carcinoma
Multigenic/multifactorial, Not applicable
All ages
Nasu-Hakola disease
Autosomal recessive
Adolescent, Adult
Nathalie syndrome
Childhood