MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Dopamine beta-hydroxylase deficiency

ORPHA:230Kr.
Autosomal recessive

Double outlet left ventricle

ORPHA:3427Morph.
Not applicable

Double outlet right ventricle

ORPHA:3426Morph.
Multigenic/multifactorial

Double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy

ORPHA:423712Kl. subt.
Multigenic/multifactorial

Double outlet right ventricle with non-committed subpulmonary ventricular septal defect

ORPHA:99046Kl. subt.
Multigenic/multifactorial

Double outlet right ventricle with subaortic or doubly committed ventricular septal defect

ORPHA:423693Kl. subt.
Multigenic/multifactorial

Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis

ORPHA:99043Kl. subt.
Multigenic/multifactorial

Double outlet right ventricle with subpulmonary ventricular septal defect

ORPHA:99045Kl. subt.
Multigenic/multifactorial

Double uterus-hemivagina-renal agenesis syndrome

ORPHA:3411Malf.
Unknown

Dowling-Degos disease

ORPHA:79145Kr.
Autosomal dominant

Down syndrome

ORPHA:870Malf.
Not applicable

Dracunculiasis

ORPHA:231Kr.

Dravet syndrome

ORPHA:33069Kr.
Autosomal dominant

Drug or radiation exposure-related interstitial lung disease

ORPHA:264978spez. Sit.

Drug reaction with eosinophilia and systemic symptoms

ORPHA:139402Kr.
Not applicable

Drug- or toxin-induced pulmonary arterial hypertension

ORPHA:275786Kl. gruppe
Multigenic/multifactorial

Drug-induced autoimmune hemolytic anemia

ORPHA:90037Kr.
Multigenic/multifactorial

Drug-induced localized lipodystrophy

ORPHA:90157Kr.

Drug-induced lupus erythematosus

ORPHA:231111Kr.
Not applicable

Drug-related renal tubular dysgenesis

ORPHA:97368Ätl. subt.
Not applicable

Duane retraction syndrome

ORPHA:233Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Duane retraction syndrome with congenital deafness

ORPHA:529574Malf.
Autosomal dominant

Dubin-Johnson syndrome

ORPHA:234Kr.
Autosomal recessive

Dubowitz syndrome

ORPHA:235Malf.
Autosomal recessive