MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome

ORPHA:293987Disease
Unknown

Rapid-onset dystonia-parkinsonism

ORPHA:71517Disease
Autosomal dominant, Not applicable

Rapidly involuting congenital hemangioma

ORPHA:141184Disease
Not applicable

Rare adenocarcinoma of the breast

ORPHA:213528Disease

Rare isolated myopia

ORPHA:98619Disease
Autosomal dominant, Autosomal recessive

Rare non-syndromic genetic deafness

ORPHA:87884Disease
Autosomal dominant, Autosomal recessive, X-linked recessive

Rare non-syndromic intellectual disability

ORPHA:101685Disease
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Rasmussen subacute encephalitis

ORPHA:1929Disease
Not applicable

Rat-bite fever

ORPHA:31205Disease

Ravine syndrome

ORPHA:99852Disease
Autosomal recessive

Reactive arthritis

ORPHA:29207Disease
Multigenic/multifactorial, Not applicable

Recessive X-linked ichthyosis

ORPHA:461Disease
X-linked recessive

Recessive dystrophic epidermolysis bullosa inversa

ORPHA:79409Disease
Autosomal recessive

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

ORPHA:280384Disease
Autosomal recessive

Recessive mitochondrial ataxia syndrome

ORPHA:94125Disease
Autosomal recessive

Recurrent Neisseria infections due to factor D deficiency

ORPHA:169467Disease
Autosomal recessive

Recurrent infections associated with rare immunoglobulin isotypes deficiency

ORPHA:183675Disease
Unknown

Recurrent infections due to specific granule deficiency

ORPHA:169142Disease
Autosomal recessive

Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome

ORPHA:480864Disease
Autosomal recessive

Recurrent respiratory papillomatosis

ORPHA:60032Disease
Not applicable

Reducing body myopathy

ORPHA:97239Disease
Not applicable, X-linked dominant

Refractory anemia with excess blasts in transformation

ORPHA:168960Disease

Refractory celiac disease

ORPHA:398063Disease
Not applicable

Regional odontodysplasia

ORPHA:83450Disease
Not applicable