MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Alpha-mannosidosis, infantile form

ORPHA:309282Kl. subt.
Autosomal recessive

Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3

ORPHA:62Kr.
Autosomal recessive

Alpha-thalassemia

ORPHA:846Kl. gruppe
Autosomal recessive

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ORPHA:98791Malf.
Not applicable, Unknown

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 rhabdomyosarcoma

ORPHA:99756Kl. subt.
Multigenic/multifactorial

Alveolar soft tissue sarcoma

ORPHA:163699Kr.
Not applicable

Amaurosis-hypertrichosis syndrome

ORPHA:1021Kr.
Autosomal recessive

Amelo-onycho-hypohidrotic syndrome

ORPHA:1028Malf.

Ameloblastic carcinoma

ORPHA:314422Kr.
Not applicable

Ameloblastoma

ORPHA:314419Kr.
Not applicable

Amelocerebrohypohidrotic syndrome

ORPHA:1946Malf.
Autosomal recessive

Amelogenesis imperfecta

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

American trypanosomiasis

ORPHA:3386Kr.
Not applicable

Aminoacylase 1 deficiency

ORPHA:137754Kr.
Autosomal recessive

Aminopterin/methotrexate embryofetopathy

ORPHA:1908Malf.
Not applicable

Amish lethal microcephaly

ORPHA:99742Malf.
Autosomal recessive

Amish nemaline myopathy

ORPHA:98902Kr.
Autosomal recessive

Amniotic band syndrome

ORPHA:295000Malf.