Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Acalvaria
Not applicable
Antenatal, Neonatal
Achalasia-microcephaly syndrome
Autosomal recessive
Neonatal
Acitretin/etretinate embryopathy
Not applicable
Antenatal, Neonatal
Acro-renal-mandibular syndrome
Autosomal recessive
Antenatal, Neonatal
Acro-renal-ocular syndrome
Autosomal dominant
Antenatal, Neonatal
Acrocallosal syndrome
Autosomal recessive
Antenatal, Neonatal
Acrocapitofemoral dysplasia
Autosomal recessive
Infancy, Neonatal
Acrocardiofacial syndrome
Autosomal recessive
Antenatal, Neonatal
Acrocephalopolydactyly
Autosomal recessive
Infancy, Neonatal
Acrocraniofacial dysostosis
Autosomal recessive
Antenatal, Neonatal
Acrodysostosis
Autosomal dominant
Antenatal, Neonatal
Acrodysplasia scoliosis
Neonatal
Acrofacial dysostosis, Catania type
Autosomal dominant, X-linked dominant
Antenatal, Neonatal
Acrofacial dysostosis, Kennedy-Teebi type
Autosomal recessive
Infancy, Neonatal
Acrofacial dysostosis, Palagonia type
Unknown
Infancy, Neonatal
Acrofacial dysostosis, Rodríguez type
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Acrofacial dysostosis, Weyers type
Autosomal dominant
Neonatal
Acrofrontofacionasal dysostosis
Autosomal recessive
Neonatal
Acrogeria
Unknown
Childhood, Infancy
Acromelic frontonasal dysplasia
Autosomal dominant
Antenatal, Neonatal
Acromesomelic dysplasia, Grebe type
Autosomal recessive
Antenatal, Neonatal
Acromesomelic dysplasia, Hunter-Thompson type
Autosomal recessive
Antenatal, Neonatal
Acromesomelic dysplasia, Maroteaux type
Autosomal recessive
Infancy, Neonatal
Acromicric dysplasia
Autosomal dominant
Neonatal