Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Distal hereditary motor neuropathy type 1
Autosomal dominant
Adolescent, Adult, Childhood
Distal hereditary motor neuropathy type 2
Autosomal dominant
Adolescent, Adult
Distal hereditary motor neuropathy type 5
Autosomal dominant
Adolescent, Adult, Childhood
Distal hereditary motor neuropathy type 7
Autosomal dominant
Adolescent, Adult, Childhood
Distal hereditary motor neuropathy, Jerash type
Autosomal recessive
Childhood
Distal limb deficiencies-micrognathia syndrome
Autosomal recessive
Neonatal
Distal monosomy 7q36 syndrome
Antenatal, Neonatal
Distal muscle weakness-foot deformity-elevated sorbitol level-hereditary motor neuropathy
Autosomal recessive
Distal myopathy
Autosomal dominant, Autosomal recessive
All ages
Distal myopathy with anterior tibial onset
Autosomal recessive
Adolescent, Adult
Distal myopathy, Tateyama type
Autosomal dominant
Adult
Distal myopathy, Welander type
Autosomal dominant
Adult
Distal myotilinopathy
Autosomal dominant
Adult, Elderly
Distal renal tubular acidosis
Autosomal dominant, Autosomal recessive, Not applicable
All ages
Distal renal tubular acidosis with anemia
Autosomal dominant
Infancy, Neonatal
Distal spinal muscular atrophy type 3
Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Distal triplication 15q syndrome
Not applicable, Unknown
Infancy, Neonatal
Distomatosis
Not applicable
All ages
Dobrow syndrome
Antenatal, Infancy, Neonatal
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Autosomal dominant
Adult
Donnai-Barrow syndrome
Autosomal recessive
Antenatal, Neonatal
Donohue syndrome
Autosomal recessive
Antenatal, Neonatal
Dopa-responsive dystonia
Autosomal dominant, Autosomal recessive, Not applicable
Childhood
Dopa-responsive dystonia due to sepiapterin reductase deficiency
Autosomal recessive
Infancy, Neonatal