MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Charcot-Marie-Tooth disease type 4B1

ORPHA:99955Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4B2

ORPHA:99956Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4B3

ORPHA:363981Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4C

ORPHA:99949Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4D

ORPHA:99950Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4E

ORPHA:99951Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4F

ORPHA:99952Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4G

ORPHA:99953Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4H

ORPHA:99954Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease type 4J

ORPHA:139515Заболевание
Autosomal recessive

Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome

ORPHA:90103Мальформация
Autosomal recessive

Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy

ORPHA:166Категория
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Charlie M syndrome

ORPHA:1406Мальформация
Not applicable

Cheilitis glandularis

ORPHA:1221Заболевание
Not applicable

Cherubism

ORPHA:184Мальформация
Autosomal dominant, Autosomal recessive, Not applicable

Chikungunya

ORPHA:324625Заболевание
Not applicable

Chilblain lupus

ORPHA:90280Заболевание
Not applicable

Childhood absence epilepsy

ORPHA:64280Заболевание
Autosomal dominant

Childhood disintegrative disorder

ORPHA:168782Заболевание
Not applicable

Childhood encephalopathy due to thiamine pyrophosphokinase deficiency

ORPHA:293955Заболевание
Autosomal recessive

Childhood-onset Steinert myotonic dystrophy

ORPHA:589824Клин. подтип
Autosomal dominant

Childhood-onset autosomal recessive myopathy with external ophthalmoplegia

ORPHA:363677Заболевание
Autosomal recessive

Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia

ORPHA:284324Заболевание
Autosomal recessive

Childhood-onset basal ganglia degeneration syndrome

ORPHA:497906Заболевание
Autosomal recessive