Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Ring chromosome 15 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 16 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 17 syndrome
Not applicable, Unknown
Childhood
Ring chromosome 18 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 19 syndrome
Antenatal
Ring chromosome 2 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 20 syndrome
Unknown
Adolescent, Adult, Childhood, Infancy
Ring chromosome 21 syndrome
Antenatal, Neonatal
Ring chromosome 22 syndrome
Infancy, Neonatal
Ring chromosome 3 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 4 syndrome
Infancy, Neonatal
Ring chromosome 5 syndrome
Not applicable, Unknown
Infancy, Neonatal
Ring chromosome 6 syndrome
Antenatal, Infancy, Neonatal
Ring chromosome 7 syndrome
Antenatal, Neonatal
Ring chromosome 8 syndrome
Antenatal, Neonatal
Ring chromosome 9 syndrome
Antenatal, Neonatal
Ring chromosome Y syndrome
Neonatal
Ring chromosome syndrome
Ring dermoid of cornea
Autosomal dominant
Infancy, Neonatal
Ringed hair disease
Autosomal dominant, Not applicable
Childhood
Rippling muscle disease
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood, Elderly, Infancy
Rippling muscle disease with myasthenia gravis
Not applicable
Roberts syndrome
Autosomal recessive
Antenatal, Neonatal
Robin sequence-oligodactyly syndrome
Neonatal