Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Oculofaciocardiodental syndrome
X-linked dominant
Infancy, Neonatal
Oculogastrointestinal muscular dystrophy
Autosomal recessive
Childhood
Oculogastrointestinal-neurodevelopmental syndrome
Autosomal recessive
Infancy, Neonatal
Oculomaxillofacial dysostosis
Neonatal
Oculoosteocutaneous syndrome
Autosomal recessive
Infancy, Neonatal
Oculootodental syndrome
Infancy
Oculopharyngeal muscular dystrophy
Autosomal dominant, Autosomal recessive
Adult, Elderly
Oculopharyngodistal myopathy
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood
Oculoskeletodental syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Oculotrichoanal syndrome
Autosomal recessive
Infancy, Neonatal
Oculotrichodysplasia
Autosomal recessive
Childhood
Odonto-onycho dysplasia-alopecia syndrome
Neonatal
Odonto-onycho-dermal dysplasia
Autosomal recessive
Childhood
Odonto-tricho-ungual-digito-palmar syndrome
Autosomal dominant
Infancy, Neonatal
Odontochondrodysplasia
Autosomal recessive
Infancy, Neonatal
Odontohypophosphatasia
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Odontoleukodystrophy
Autosomal recessive
Infancy
Odontomatosis-aortae esophagus stenosis syndrome
No data available
Odontomicronychial dysplasia
Autosomal recessive
Childhood
Odontotrichomelic syndrome
Autosomal recessive
Childhood
Off-periods in Parkinson disease not responding to oral treatment
Not applicable
Adult, Elderly
Ogden syndrome
X-linked dominant, X-linked recessive
Infancy, Neonatal
Oguchi disease
Autosomal recessive
Infancy, Neonatal
Okihiro syndrome
Autosomal dominant
Neonatal