MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Digital extensor muscle aplasia-polyneuropathy

ORPHA:2926Мальформация

Digitalis poisoning

ORPHA:31828Особая клин. ситуация
Not applicable

Dihydropteridine reductase deficiency

ORPHA:226Клин. подтип
Autosomal recessive

Dihydropyrimidine dehydrogenase deficiency

ORPHA:1675Заболевание
Autosomal recessive

Dihydropyrimidinuria

ORPHA:38874Заболевание
Autosomal recessive

Dilated cardiomyopathy

ORPHA:217604Категория

Dilated cardiomyopathy with ataxia

ORPHA:66634Заболевание
Autosomal recessive

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

ORPHA:2229Мальформация
Autosomal recessive

Dimethylglycine dehydrogenase deficiency

ORPHA:243343Заболевание
Autosomal recessive

Diphallia

ORPHA:227Морф. аномалия

Diphtheria

ORPHA:1679Заболевание

Diphyllobothriasis

ORPHA:128Заболевание
Not applicable

Diprosopus

ORPHA:1681Морф. аномалия
No data available

Dirofilariasis

ORPHA:166291Заболевание
Not applicable

Discoid lupus erythematosus

ORPHA:90281Заболевание

Dislocation of the hip-dysmorphism syndrome

ORPHA:2412Мальформация
Autosomal recessive

Disorder of bile acid synthesis

ORPHA:79168Категория

Disorder of the gamma-glutamyl cycle

ORPHA:79196Категория
Autosomal recessive

Disorder of thiamine metabolism and transport

ORPHA:298644Категория
Autosomal dominant, Autosomal recessive

Dissecting cellulitis of the scalp

ORPHA:345Заболевание
Not applicable

Disseminated peritoneal leiomyomatosis

ORPHA:71274Заболевание
Unknown

Disseminated superficial actinic porokeratosis

ORPHA:79152Заболевание
Autosomal dominant

Distal 16p11.2 microdeletion syndrome

ORPHA:261222Мальформация
Not applicable

Distal 17p13.1 microdeletion syndrome

ORPHA:319171Мальформация
Not applicable