MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Adult hypophosphatasia

ORPHA:247676Clin. sub.
Autosomal dominant, Autosomal recessive

Adult idiopathic neutropenia

ORPHA:2688Disease
Not applicable

Adult intestinal botulism

ORPHA:178487Clin. sub.

Adult polyglucosan body disease

ORPHA:206583Clin. sub.
Autosomal recessive

Adult-onset Steinert myotonic dystrophy

ORPHA:589830Clin. sub.
Autosomal dominant

Adult-onset Still disease

ORPHA:829Disease
Not applicable

Adult-onset autosomal dominant leukodystrophy

ORPHA:99027Disease
Autosomal dominant

Adult-onset autosomal recessive cerebellar ataxia

ORPHA:284289Disease
Autosomal recessive

Adult-onset autosomal recessive sideroblastic anemia

ORPHA:255132Disease
Autosomal recessive

Adult-onset cervical dystonia, DYT23 type

ORPHA:420492Disease
Autosomal dominant

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

ORPHA:329336Disease
Autosomal dominant, Mitochondrial inheritance

Adult-onset common variable immunodeficiency due to BAFF-receptor deficiency

ORPHA:696925Disease
Autosomal recessive

Adult-onset distal myopathy due to VCP mutation

ORPHA:329478Disease
Autosomal dominant

Adult-onset dystonia-parkinsonism

ORPHA:199351Disease
Autosomal recessive

Adult-onset foveomacular vitelliform dystrophy

ORPHA:99000Disease
Autosomal dominant, Not applicable

Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies

ORPHA:306431Disease
Not applicable

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

ORPHA:313808Disease
Autosomal dominant

Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

ORPHA:329314Disease
Autosomal recessive

Adult-onset myasthenia gravis

ORPHA:391490Clin. sub.
Multigenic/multifactorial, Not applicable

Adult-onset nemaline myopathy

ORPHA:171442Disease
Not applicable

Adult-onset progressive leukoencephalopathy-early-onset deafness

ORPHA:652532Disease
Autosomal recessive

African tick typhus

ORPHA:101334Disease
Not applicable

African trypanosomiasis

ORPHA:3385Disease
Not applicable

Agammaglobulinemia

ORPHA:183669Cat.