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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Feingold syndrome type 2

ORPHA:391646Clin. sub.
Autosomal dominant

Felty syndrome

ORPHA:47612Disease
Unknown

Female infertility due to oocyte meiotic arrest

ORPHA:488191Disease
Autosomal recessive

Female infertility due to zona pellucida defect

ORPHA:404466Disease
Autosomal dominant, Autosomal recessive

Femoral-facial syndrome

ORPHA:1988Malform.
Not applicable

Femur-fibula-ulna complex

ORPHA:2019Malform.
Not applicable

Ferro-cerebro-cutaneous syndrome

ORPHA:397922Disease
X-linked recessive

Ferroportin disease

ORPHA:648562Disease

Fetal Gaucher disease

ORPHA:85212Clin. sub.
Autosomal recessive

Fetal akinesia deformation sequence

ORPHA:994Malform.
Autosomal recessive

Fetal akinesia-cerebral and retinal hemorrhage syndrome

ORPHA:363409Disease
Autosomal recessive

Fetal alcohol syndrome

ORPHA:1915Malform.
Not applicable

Fetal and neonatal alloimmune thrombocytopenia

ORPHA:853Disease
Not applicable

Fetal carbamazepine syndrome

ORPHA:370076Malform.
Not applicable

Fetal cytomegalovirus syndrome

ORPHA:294Disease
Not applicable

Fetal encasement syndrome

ORPHA:465824Malform.
Autosomal recessive

Fetal hydantoin syndrome

ORPHA:1912Malform.
Not applicable

Fetal iodine syndrome

ORPHA:1910Malform.
Not applicable

Fetal lung interstitial tumor

ORPHA:284362Clin. sub.

Fetal methylmercury syndrome

ORPHA:1917Malform.
Not applicable

Fetal minoxidil syndrome

ORPHA:1918Malform.
Not applicable

Fetal parvovirus syndrome

ORPHA:295Malform.
Not applicable

Fetal trimethadione syndrome

ORPHA:1913Malform.
Not applicable

Fetal valproate spectrum disorder

ORPHA:1906Malform.
Not applicable