Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Müllerian aplasia
Autosomal dominant
Adolescent, Adult
NLRP3-associated autoinflammatory disease
Autosomal dominant, Not applicable
Adolescent, Childhood, Infancy, Neonatal
Nemaline myopathy
Autosomal dominant, Autosomal recessive, Not applicable
All ages
Neuroacanthocytosis
Neurodegeneration with brain iron accumulation
Autosomal dominant, Autosomal recessive, X-linked dominant
Adolescent, Adult, Childhood, Infancy
Neuronal ceroid lipofuscinosis
Autosomal dominant, Autosomal recessive
All ages
Neutral lipid storage disease
Autosomal recessive
Infancy, Neonatal
Non-histaminic angioedema
Autosomal dominant, Not applicable
All ages
Non-rhizomelic chondrodysplasia punctata
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive
Infancy, Neonatal
Non-syndromic anorectal malformation
Antenatal, Neonatal
Non-syndromic craniosynostosis
Infancy, Neonatal
Non-syndromic hemimelia
Not applicable
Neonatal
Non-syndromic pontocerebellar hypoplasia
Autosomal recessive
Antenatal, Infancy, Neonatal
Oblique facial cleft
Infancy, Neonatal
Oculocutaneous albinism
Autosomal recessive
Neonatal
Oligoastrocytic tumor
Oligodendroglial tumor
Multigenic/multifactorial, Not applicable
Adult
Open spinal dysraphism
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Oromandibular-limb hypogenesis syndrome
Infancy, Neonatal
Osteopetrosis and related disorders
Autosomal dominant, Autosomal recessive, X-linked recessive
All ages
Paramedian facial cleft
Antenatal, Neonatal
Paroxysmal dyskinesia
Autosomal dominant, Not applicable
Childhood
Peeling skin syndrome
Autosomal recessive
Infancy, Neonatal
Peroxisome biogenesis disorder
Autosomal recessive
Infancy, Neonatal