MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Hemolytic anemia due to adenylate kinase deficiency

ORPHA:86817Kr.
Autosomal recessive

Hemolytic anemia due to diphosphoglycerate mutase deficiency

ORPHA:714Kr.
Autosomal recessive

Hemolytic anemia due to erythrocyte adenosine deaminase overproduction

ORPHA:99138Kr.
Autosomal dominant

Hemolytic anemia due to glucophosphate isomerase deficiency

ORPHA:712Kr.
Autosomal recessive

Hemolytic anemia due to glutathione reductase deficiency

ORPHA:90030Kr.
Autosomal recessive

Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency

ORPHA:35120Kr.
Autosomal recessive

Hemolytic anemia due to red cell pyruvate kinase deficiency

ORPHA:766Kr.
Autosomal recessive

Hemolytic disease of the newborn with Kell alloimmunization

ORPHA:275944Kr.

Hemolytic uremic syndrome with DGKE deficiency

ORPHA:357008Kr.
Autosomal recessive, Not applicable

Hemophagocytic syndrome

ORPHA:158032Kat.

Hemophagocytic syndrome associated with an infection

ORPHA:158048spez. Sit.

Hemophilia

ORPHA:448Kl. gruppe
X-linked recessive

Hemophilia A

ORPHA:98878Kr.
X-linked recessive

Hemophilia B

ORPHA:98879Kr.
X-linked recessive

Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

ORPHA:178396Kr.
Autosomal dominant, Not applicable

Hemorrhagic fever-renal syndrome

ORPHA:340Kr.
Not applicable

Hendra virus infection

ORPHA:324632Kr.

Hennekam syndrome

ORPHA:2136Malf.
Autosomal recessive

Hepatic arteriovenous malformation

ORPHA:693846Malf.
Not applicable

Hepatic fibrosis-renal cysts-intellectual disability syndrome

ORPHA:2031Malf.

Hepatic veno-occlusive disease

ORPHA:890Kr.
Not applicable

Hepatic veno-occlusive disease-immunodeficiency syndrome

ORPHA:79124Kr.
Autosomal recessive

Hepatitis B reinfection following liver transplantation

ORPHA:90073spez. Sit.
Not applicable

Hepatitis delta

ORPHA:402823Kr.
Not applicable