Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Adult hypophosphatasia
Autosomal dominant, Autosomal recessive
Adult
Adult idiopathic neutropenia
Not applicable
Adult
Adult intestinal botulism
Adult
Adult polyglucosan body disease
Autosomal recessive
Adult
Adult-onset Steinert myotonic dystrophy
Autosomal dominant
Adult
Adult-onset Still disease
Not applicable
Adult, Elderly
Adult-onset autosomal dominant leukodystrophy
Autosomal dominant
Adult
Adult-onset autosomal recessive cerebellar ataxia
Autosomal recessive
Adult
Adult-onset autosomal recessive sideroblastic anemia
Autosomal recessive
Adult
Adult-onset cervical dystonia, DYT23 type
Autosomal dominant
Adult
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant, Mitochondrial inheritance
Adult
Adult-onset common variable immunodeficiency due to BAFF-receptor deficiency
Autosomal recessive
Adult-onset distal myopathy due to VCP mutation
Autosomal dominant
Adult
Adult-onset dystonia-parkinsonism
Autosomal recessive
Adolescent, Adult
Adult-onset foveomacular vitelliform dystrophy
Autosomal dominant, Not applicable
Adult
Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies
Not applicable
Adult
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Autosomal dominant
Adult
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
Autosomal recessive
Adult
Adult-onset myasthenia gravis
Multigenic/multifactorial, Not applicable
Adult
Adult-onset nemaline myopathy
Not applicable
Adult
Adult-onset progressive leukoencephalopathy-early-onset deafness
Autosomal recessive
Adult
African tick typhus
Not applicable
African trypanosomiasis
Not applicable
All ages