MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Benign recurrent intrahepatic cholestasis type 1

ORPHA:99960Клин. под.
Autosomal recessive

Benign recurrent intrahepatic cholestasis type 2

ORPHA:99961Клин. под.
Autosomal recessive

Benign schwannoma

ORPHA:252164Ауру
Not applicable

Bernard-Soulier syndrome

ORPHA:274Ауру
Autosomal dominant, Autosomal recessive

Best vitelliform macular dystrophy

ORPHA:1243Ауру
Autosomal dominant

Beta-ketothiolase deficiency

ORPHA:134Ауру
Autosomal recessive

Beta-mannosidosis

ORPHA:118Ауру
Autosomal recessive

Beta-mercaptolactate cysteine disulfiduria

ORPHA:1035Био аном.

Beta-propeller protein-associated neurodegeneration

ORPHA:329284Ауру
X-linked dominant

Beta-sarcoglycan-related limb-girdle muscular dystrophy R4

ORPHA:119Ауру
Autosomal recessive

Beta-thalassemia

ORPHA:848Клин. топ
Autosomal dominant, Autosomal recessive

Beta-thalassemia associated with another hemoglobin anomaly

ORPHA:231230Сан.
Autosomal dominant, Autosomal recessive

Beta-thalassemia intermedia

ORPHA:231222Ауру
Autosomal recessive

Beta-thalassemia major

ORPHA:231214Ауру
Autosomal recessive

Beta-thalassemia-X-linked thrombocytopenia syndrome

ORPHA:231393Ауру
X-linked recessive

Beta-ureidopropionase deficiency

ORPHA:65287Ауру
Autosomal recessive

Bethlem muscular dystrophy

ORPHA:610Ауру
Autosomal dominant, Autosomal recessive

Bickerstaff brainstem encephalitis

ORPHA:79138Ауру
Not applicable

Biemond syndrome type 2

ORPHA:141333Ауру
Unknown

Bietti crystalline dystrophy

ORPHA:41751Ауру
Autosomal recessive

Bifid nose

ORPHA:2695Мальф.
Autosomal dominant, Autosomal recessive

Bifid uvula

ORPHA:99771Морф.
Multigenic/multifactorial, Not applicable

Bifunctional enzyme deficiency

ORPHA:300Ауру
Autosomal recessive

Bilateral acute depigmentation of the iris

ORPHA:69736Ауру
Unknown