Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
NEK9-related lethal skeletal dysplasia
Autosomal recessive
Antenatal
NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome
X-linked recessive
NPHP3-related Meckel-like syndrome
Autosomal recessive
Childhood
NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance
Autosomal recessive
Neonatal
Nager syndrome
Autosomal dominant, Autosomal recessive, Not applicable
Antenatal, Neonatal
Nail-patella syndrome
Autosomal dominant
Antenatal, Childhood, Infancy, Neonatal
Nance-Horan syndrome
X-linked dominant
Neonatal
Nanophthalmos
Autosomal dominant, Autosomal recessive, Not applicable
Infancy, Neonatal
Nasopalpebral lipoma-coloboma syndrome
Autosomal dominant
Neonatal
Nasu-Hakola disease
Autosomal recessive
Adolescent, Adult
Nathalie syndrome
Childhood
Native American myopathy
Autosomal recessive
Infancy, Neonatal
Nephropathy-deafness-hyperparathyroidism syndrome
Autosomal recessive
Childhood
Nephrosis-deafness-urinary tract-digital malformations syndrome
Unknown
Infancy, Neonatal
Nestor-Guillermo progeria syndrome
Autosomal recessive
Childhood
Neu-Laxova syndrome
Autosomal recessive
Antenatal
Neuhauser-Eichner-Opitz syndrome
Autosomal dominant
Childhood, Infancy
Neurodevelopmental delay-brain malformations-skeletal defects-intellectual disability syndrome
Autosomal dominant
Infancy
Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome
Autosomal dominant
Neurodevelopmental delay-intellectual disability-skeletal defects syndrome
X-linked dominant
Infancy, Neonatal
Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome
Autosomal recessive
Infancy
Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome
Autosomal dominant
Infancy, Neonatal
Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome
Autosomal dominant, Not applicable
Antenatal, Infancy, Neonatal
Neurodevelopmental disorder-slit-like lateral ventricles-intellectual disability syndrome
Autosomal recessive