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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 218 заболеваний (Клин. гр.) Сброс

Carcinoma of gallbladder and extrahepatic biliary tract

ORPHA:56044Клин. гр.
Not applicable

Central congenital hypothyroidism

ORPHA:226298Клин. гр.

Central nervous system embryonal tumor

ORPHA:251870Клин. гр.
Not applicable

Centronuclear myopathy

ORPHA:595Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Cephalocele

ORPHA:268817Клин. гр.

Cerebral cortical dysplasia

ORPHA:268950Клин. гр.

Charcot-Marie-Tooth disease type 1

ORPHA:65753Клин. гр.
Autosomal dominant

Charcot-Marie-Tooth disease type 4

ORPHA:64749Клин. гр.
Autosomal recessive

Choroid plexus tumor

ORPHA:251896Клин. гр.

Chronic cutaneous lupus erythematosus

ORPHA:163531Клин. гр.
Multigenic/multifactorial

Cleft lip with or without cleft palate

ORPHA:1991Клин. гр.

Cleft palate

ORPHA:2014Клин. гр.
Multigenic/multifactorial, Not applicable

Cobblestone lissencephaly

ORPHA:51577Клин. гр.
Autosomal recessive

Coenzyme Q10 deficiency

ORPHA:35656Клин. гр.
Autosomal recessive

Cold-induced sweating syndrome-hyperthermia spectrum

ORPHA:401993Клин. гр.
Autosomal recessive

Congenital adrenal hyperplasia

ORPHA:418Клин. гр.
Autosomal recessive

Congenital dyserythropoietic anemia

ORPHA:85Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Congenital isolated hyperinsulinism

ORPHA:657Клин. гр.
Autosomal dominant, Autosomal recessive

Congenital long QT syndrome

ORPHA:768Клин. гр.
Autosomal dominant, Autosomal recessive

Congenital myotonia

ORPHA:206973Клин. гр.

Congenital pulmonary veins atresia or stenosis

ORPHA:3188Клин. гр.
Not applicable

Congenital stationary night blindness

ORPHA:215Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Creatine deficiency syndrome

ORPHA:79172Клин. гр.
Autosomal recessive, Not applicable, X-linked recessive

Cutaneous mastocytosis

ORPHA:66646Клин. гр.
Not applicable