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

Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome

ORPHA:1014Kr.
Unknown

Alpers-Huttenlocher syndrome

ORPHA:726Kr.
Autosomal recessive

Alpha delta granule deficiency

ORPHA:734Kr.
Autosomal dominant, Autosomal recessive

Alpha-1-antitrypsin deficiency

ORPHA:60Kr.
Autosomal recessive

Alpha-B crystallin-related late-onset myopathy

ORPHA:399058Kr.
Autosomal dominant

Alpha-N-acetylgalactosaminidase deficiency

ORPHA:3137Kr.
Autosomal recessive

Alpha-dystroglycan-related limb-girdle muscular dystrophy R16

ORPHA:280333Kr.
Autosomal recessive

Alpha-mannosidosis

ORPHA:61Kr.
Autosomal recessive

Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3

ORPHA:62Kr.
Autosomal recessive

Alpha-thalassemia-myelodysplastic syndrome

ORPHA:231401Kr.
Not applicable

Alport syndrome

ORPHA:63Kr.
Autosomal dominant, Autosomal recessive, X-linked dominant

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

ORPHA:86818Kr.
X-linked recessive

Alström syndrome

ORPHA:64Kr.
Autosomal recessive

Alternating hemiplegia of childhood

ORPHA:2131Kr.
Autosomal dominant, Not applicable

Alveolar echinococcosis

ORPHA:284Kr.
Not applicable

Alveolar soft tissue sarcoma

ORPHA:163699Kr.
Not applicable

Amaurosis-hypertrichosis syndrome

ORPHA:1021Kr.
Autosomal recessive

Ameloblastic carcinoma

ORPHA:314422Kr.
Not applicable

Ameloblastoma

ORPHA:314419Kr.
Not applicable

Amelogenesis imperfecta

ORPHA:88661Kr.
Autosomal dominant, Autosomal recessive, X-linked dominant

American trypanosomiasis

ORPHA:3386Kr.
Not applicable

Aminoacylase 1 deficiency

ORPHA:137754Kr.
Autosomal recessive

Amish nemaline myopathy

ORPHA:98902Kr.
Autosomal recessive

Amniotic fluid embolism

ORPHA:617304Kr.