Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Acrootoocular syndrome
Autosomal recessive
Infancy, Neonatal
Acropectoral syndrome
Autosomal dominant
Infancy, Neonatal
Acropectorovertebral dysplasia
Autosomal dominant
Antenatal, Neonatal
Acrorenal syndrome
Autosomal recessive
Neonatal
Adams-Oliver syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Adducted thumbs-arthrogryposis syndrome, Christian type
Autosomal recessive
Neonatal
Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Agnathia-holoprosencephaly-situs inversus syndrome
Autosomal dominant, Autosomal recessive, Not applicable
Antenatal, Neonatal
Alagille syndrome
Autosomal dominant
All ages
Alar cartilages hypoplasia-coloboma-telecanthus syndrome
Autosomal recessive
Neonatal
Alazami syndrome
Autosomal recessive
Antenatal, Neonatal
Alazami-Yuan syndrome
Autosomal recessive
Albers-Schönberg osteopetrosis
Autosomal dominant
Childhood
Albinism-deafness syndrome
X-linked recessive
Neonatal
Alopecia-contractures-dwarfism-intellectual disability syndrome
Autosomal recessive
Antenatal, Neonatal
Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
Not applicable, Unknown
Infancy, Neonatal
Amelo-onycho-hypohidrotic syndrome
No data available
Amelocerebrohypohidrotic syndrome
Autosomal recessive
Childhood, Infancy, Neonatal
Aminopterin/methotrexate embryofetopathy
Not applicable
Antenatal, Neonatal
Amish lethal microcephaly
Autosomal recessive
Antenatal, Infancy, Neonatal
Amniotic band syndrome
Antenatal, Neonatal
Angel-shaped phalango-epiphyseal dysplasia
Autosomal dominant
All ages
Angelman syndrome
Not applicable
Infancy
Aniridia-absent patella syndrome
Autosomal dominant
Antenatal, Neonatal