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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Benign recurrent intrahepatic cholestasis type 1

ORPHA:99960Clin. sub.
Autosomal recessive

Benign recurrent intrahepatic cholestasis type 2

ORPHA:99961Clin. sub.
Autosomal recessive

Benign schwannoma

ORPHA:252164Disease
Not applicable

Bernard-Soulier syndrome

ORPHA:274Disease
Autosomal dominant, Autosomal recessive

Best vitelliform macular dystrophy

ORPHA:1243Disease
Autosomal dominant

Beta-ketothiolase deficiency

ORPHA:134Disease
Autosomal recessive

Beta-mannosidosis

ORPHA:118Disease
Autosomal recessive

Beta-mercaptolactate cysteine disulfiduria

ORPHA:1035Bio anom.

Beta-propeller protein-associated neurodegeneration

ORPHA:329284Disease
X-linked dominant

Beta-sarcoglycan-related limb-girdle muscular dystrophy R4

ORPHA:119Disease
Autosomal recessive

Beta-thalassemia

ORPHA:848Clin. grp.
Autosomal dominant, Autosomal recessive

Beta-thalassemia associated with another hemoglobin anomaly

ORPHA:231230Cat.
Autosomal dominant, Autosomal recessive

Beta-thalassemia intermedia

ORPHA:231222Disease
Autosomal recessive

Beta-thalassemia major

ORPHA:231214Disease
Autosomal recessive

Beta-thalassemia-X-linked thrombocytopenia syndrome

ORPHA:231393Disease
X-linked recessive

Beta-ureidopropionase deficiency

ORPHA:65287Disease
Autosomal recessive

Bethlem muscular dystrophy

ORPHA:610Disease
Autosomal dominant, Autosomal recessive

Bickerstaff brainstem encephalitis

ORPHA:79138Disease
Not applicable

Biemond syndrome type 2

ORPHA:141333Disease
Unknown

Bietti crystalline dystrophy

ORPHA:41751Disease
Autosomal recessive

Bifid nose

ORPHA:2695Malform.
Autosomal dominant, Autosomal recessive

Bifid uvula

ORPHA:99771Morph.
Multigenic/multifactorial, Not applicable

Bifunctional enzyme deficiency

ORPHA:300Disease
Autosomal recessive

Bilateral acute depigmentation of the iris

ORPHA:69736Disease
Unknown