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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Dopamine beta-hydroxylase deficiency

ORPHA:230Disease
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:423712Clin. sub.
Multigenic/multifactorial

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

ORPHA:99046Clin. sub.
Multigenic/multifactorial

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

ORPHA:423693Clin. sub.
Multigenic/multifactorial

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

ORPHA:99043Clin. sub.
Multigenic/multifactorial

Double outlet right ventricle with subpulmonary ventricular septal defect

ORPHA:99045Clin. sub.
Multigenic/multifactorial

Double uterus-hemivagina-renal agenesis syndrome

ORPHA:3411Malform.
Unknown

Dowling-Degos disease

ORPHA:79145Disease
Autosomal dominant

Down syndrome

ORPHA:870Malform.
Not applicable

Dracunculiasis

ORPHA:231Disease

Dravet syndrome

ORPHA:33069Disease
Autosomal dominant

Drug or radiation exposure-related interstitial lung disease

ORPHA:264978Situation

Drug reaction with eosinophilia and systemic symptoms

ORPHA:139402Disease
Not applicable

Drug- or toxin-induced pulmonary arterial hypertension

ORPHA:275786Clin. grp.
Multigenic/multifactorial

Drug-induced autoimmune hemolytic anemia

ORPHA:90037Disease
Multigenic/multifactorial

Drug-induced localized lipodystrophy

ORPHA:90157Disease

Drug-induced lupus erythematosus

ORPHA:231111Disease
Not applicable

Drug-related renal tubular dysgenesis

ORPHA:97368Etio. sub.
Not applicable

Duane retraction syndrome

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

Duane retraction syndrome with congenital deafness

ORPHA:529574Malform.
Autosomal dominant

Dubin-Johnson syndrome

ORPHA:234Disease
Autosomal recessive

Dubowitz syndrome

ORPHA:235Malform.
Autosomal recessive