Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Aseptic abscess syndrome
Not applicable
Adolescent, Adult
Asherman syndrome
Not applicable
Adult
Aspartylglucosaminuria
Autosomal recessive
Childhood
Aspergillosis
Not applicable
All ages
Astley-Kendall dysplasia
Autosomal recessive
Antenatal, Neonatal
Astroblastoma
Not applicable
Adolescent, Adult, Childhood, Infancy
Astrocytoma
All ages
Asymptomatic hyperCKemia-myalgia-rhabdomyolysis syndrome
Autosomal recessive
Ataxia with vitamin E deficiency
Autosomal recessive
All ages
Ataxia-deafness-intellectual disability syndrome
Unknown
Childhood, Infancy
Ataxia-hypogonadism-choroidal dystrophy syndrome
Autosomal recessive
Childhood
Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome
Autosomal recessive
Infancy, Neonatal
Ataxia-oculomotor apraxia type 1
Autosomal recessive
Childhood
Ataxia-oculomotor apraxia type 4
Autosomal recessive
Childhood, Infancy
Ataxia-pancytopenia syndrome
Autosomal dominant
Adolescent, Adult, Childhood
Ataxia-photosensitivity-short stature syndrome
Unknown
Childhood, Infancy
Ataxia-tapetoretinal degeneration syndrome
Unknown
Adolescent, Childhood, Infancy
Ataxia-telangiectasia
Autosomal recessive
Childhood, Infancy
Ataxia-telangiectasia variant
Autosomal recessive
Ataxia-telangiectasia-like disorder
Autosomal recessive
Infancy, Neonatal
Atelosteogenesis type I
Autosomal dominant
Antenatal, Neonatal
Atelosteogenesis type II
Autosomal recessive
Infancy, Neonatal
Atelosteogenesis type III
Autosomal dominant, Not applicable
Antenatal, Infancy, Neonatal
Athabaskan brainstem dysgenesis syndrome
Autosomal recessive
Infancy, Neonatal