MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

Acrootoocular syndrome

ORPHA:2980Malf.
Autosomal recessive

Acropectoral syndrome

ORPHA:85203Malf.
Autosomal dominant

Acropectorovertebral dysplasia

ORPHA:957Malf.
Autosomal dominant

Acrorenal syndrome

ORPHA:971Malf.
Autosomal recessive

Adams-Oliver syndrome

ORPHA:974Malf.
Autosomal dominant, Autosomal recessive

Adducted thumbs-arthrogryposis syndrome, Christian type

ORPHA:2952Malf.
Autosomal recessive

Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome

ORPHA:83617Malf.
Autosomal recessive

Agnathia-holoprosencephaly-situs inversus syndrome

ORPHA:990Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Alagille syndrome

ORPHA:52Malf.
Autosomal dominant

Alar cartilages hypoplasia-coloboma-telecanthus syndrome

ORPHA:2007Malf.
Autosomal recessive

Alazami syndrome

ORPHA:319671Malf.
Autosomal recessive

Alazami-Yuan syndrome

ORPHA:694946Malf.
Autosomal recessive

Albers-Schönberg osteopetrosis

ORPHA:53Malf.
Autosomal dominant

Albinism-deafness syndrome

ORPHA:998Malf.
X-linked recessive

Alopecia-contractures-dwarfism-intellectual disability syndrome

ORPHA:1005Malf.
Autosomal recessive

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ORPHA:98791Malf.
Not applicable, Unknown

Amelo-onycho-hypohidrotic syndrome

ORPHA:1028Malf.

Amelocerebrohypohidrotic syndrome

ORPHA:1946Malf.
Autosomal recessive

Aminopterin/methotrexate embryofetopathy

ORPHA:1908Malf.
Not applicable

Amish lethal microcephaly

ORPHA:99742Malf.
Autosomal recessive

Amniotic band syndrome

ORPHA:295000Malf.

Angel-shaped phalango-epiphyseal dysplasia

ORPHA:63442Malf.
Autosomal dominant

Angelman syndrome

ORPHA:72Malf.
Not applicable

Aniridia-absent patella syndrome

ORPHA:1069Malf.
Autosomal dominant