MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Acute peripheral arterial occlusion

ORPHA:90064Situation
Not applicable

Acute poisoning by drugs with membrane-stabilizing effect

ORPHA:43119Situation
Not applicable

Acute promyelocytic leukemia

ORPHA:520Disease
Not applicable

Acute pure sensory neuropathy

ORPHA:231450Disease
Multigenic/multifactorial, Not applicable

Acute radiation syndrome

ORPHA:454831Situation
Not applicable

Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate

ORPHA:615964Disease

Acute sensory ataxic neuropathy

ORPHA:231466Disease
Multigenic/multifactorial, Not applicable

Acute transverse myelitis

ORPHA:139417Disease

Acute transverse myelitis with anti-MOG antibodies

ORPHA:592873Clin. sub.

Acute tricyclic antidepressant poisoning

ORPHA:43117Situation
Not applicable

Acute undifferentiated leukemia

ORPHA:98835Disease

Acute zonal occult outer retinopathy

ORPHA:284454Disease
Not applicable

Acyl-CoA dehydrogenase 9 deficiency

ORPHA:99901Disease
Autosomal recessive

Adamantinoma

ORPHA:55881Disease
Not applicable

Adams-Oliver syndrome

ORPHA:974Malform.
Autosomal dominant, Autosomal recessive

Addison disease

ORPHA:85138Disease
Not applicable

Adducted thumbs-arthrogryposis syndrome, Christian type

ORPHA:2952Malform.
Autosomal recessive

Adenine phosphoribosyltransferase deficiency

ORPHA:976Disease
Autosomal recessive

Adenocarcinoma of ovary

ORPHA:213504Disease
Not applicable

Adenocarcinoma of the anal canal

ORPHA:424016Disease
Not applicable

Adenocarcinoma of the cervix uteri

ORPHA:213772Disease
Not applicable

Adenocarcinoma of the gallbladder and extrahepatic biliary tract

ORPHA:424991Disease
Not applicable

Adenocarcinoma of the liver and intrahepatic biliary tract

ORPHA:424943Disease
Not applicable

Adenocarcinoma of the oesophagus and oesophagogastric junction

ORPHA:99976Disease
Not applicable