MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Adenylosuccinate lyase deficiency

ORPHA:46Kr.
Autosomal recessive

Adenylosuccinate synthetase-like 1-related distal myopathy

ORPHA:482601Kr.
Autosomal recessive

Adiposis dolorosa

ORPHA:36397Kr.
Autosomal dominant, Not applicable

Adrenocortical carcinoma

ORPHA:1501Kr.
Not applicable

Adrenocortical carcinoma with pure aldosterone hypersecretion

ORPHA:231625Kr.
Not applicable

Adrenomyodystrophy

ORPHA:977Kr.
Unknown

Adult Refsum disease

ORPHA:773Kr.
Autosomal recessive

Adult T-cell leukemia/lymphoma

ORPHA:86875Kr.
Multigenic/multifactorial, Not applicable

Adult acute respiratory distress syndrome

ORPHA:70578Kr.
Not applicable

Adult familial nephronophthisis-spastic quadriparesia syndrome

ORPHA:2666Kr.
Unknown

Adult hepatocellular carcinoma

ORPHA:210159Kr.
Not applicable

Adult idiopathic neutropenia

ORPHA:2688Kr.
Not applicable

Adult-onset Still disease

ORPHA:829Kr.
Not applicable

Adult-onset autosomal dominant leukodystrophy

ORPHA:99027Kr.
Autosomal dominant

Adult-onset autosomal recessive cerebellar ataxia

ORPHA:284289Kr.
Autosomal recessive

Adult-onset autosomal recessive sideroblastic anemia

ORPHA:255132Kr.
Autosomal recessive

Adult-onset cervical dystonia, DYT23 type

ORPHA:420492Kr.
Autosomal dominant

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

ORPHA:329336Kr.
Autosomal dominant, Mitochondrial inheritance

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

ORPHA:696925Kr.
Autosomal recessive

Adult-onset distal myopathy due to VCP mutation

ORPHA:329478Kr.
Autosomal dominant

Adult-onset dystonia-parkinsonism

ORPHA:199351Kr.
Autosomal recessive

Adult-onset foveomacular vitelliform dystrophy

ORPHA:99000Kr.
Autosomal dominant, Not applicable

Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies

ORPHA:306431Kr.
Not applicable

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

ORPHA:313808Kr.
Autosomal dominant