MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
727 diseases matched (Clin. sub.) Reset

Acute endophthalmitis

ORPHA:279888Clin. sub.
Not applicable

Acute mast cell leukemia

ORPHA:566393Clin. sub.
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Clin. sub.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Clin. sub.
Not applicable

Acute neonatal citrullinemia type I

ORPHA:247546Clin. sub.
Autosomal recessive

Acute transverse myelitis with anti-MOG antibodies

ORPHA:592873Clin. sub.

Adrenomyeloneuropathy

ORPHA:139399Clin. sub.
X-linked recessive

Adult CLN1 disease

ORPHA:699745Clin. sub.
Autosomal recessive

Adult CLN5 disease

ORPHA:699812Clin. sub.
Autosomal recessive

Adult CLN6 disease

ORPHA:700477Clin. sub.
Autosomal recessive

Adult Krabbe disease

ORPHA:206448Clin. sub.
Autosomal recessive

Adult hypophosphatasia

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

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 myasthenia gravis

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

Alexander disease type I

ORPHA:363717Clin. sub.
Not applicable

Alexander disease type II

ORPHA:363722Clin. sub.
Autosomal dominant

Alobar holoprosencephaly

ORPHA:93925Clin. sub.
Multigenic/multifactorial, Not applicable

Alpha-N-acetylgalactosaminidase deficiency type 1

ORPHA:79279Clin. sub.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 2

ORPHA:79280Clin. sub.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 3

ORPHA:79281Clin. sub.
Autosomal recessive

Alpha-heavy chain disease

ORPHA:100025Clin. sub.

Alpha-mannosidosis, adult form

ORPHA:309288Clin. sub.
Autosomal recessive