MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Childhood-onset benign chorea with striatal involvement

ORPHA:494541Заболевание
Autosomal dominant

Childhood-onset common variable immunodeficiency due to ARHGEF1 deficiency

ORPHA:696942Заболевание
Autosomal recessive

Childhood-onset hypophosphatasia

ORPHA:247667Клин. подтип
Autosomal dominant, Autosomal recessive

Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder

ORPHA:500180Заболевание
Autosomal dominant

Childhood-onset nemaline myopathy

ORPHA:171439Заболевание
Autosomal dominant

Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome

ORPHA:466921Заболевание
Autosomal recessive

Childhood-onset schizophrenia

ORPHA:641496Заболевание

Childhood-onset spasticity with hyperglycinemia

ORPHA:401866Заболевание
Autosomal recessive

Childhood-onset stress-induced neurodegenerative ataxia-seizure syndrome

ORPHA:694922Заболевание
Autosomal recessive

Choanal atresia

ORPHA:137914Морф. аномалия
Not applicable

Choanal atresia, bilateral

ORPHA:137920Клин. подтип
Not applicable

Choanal atresia, unilateral

ORPHA:137917Клин. подтип
Not applicable

Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome

ORPHA:589856Мальформация
Autosomal dominant

Cholangiocarcinoma

ORPHA:70567Заболевание
Not applicable

Choledochal cyst

ORPHA:480501Морф. аномалия

Cholera

ORPHA:173Заболевание
Not applicable

Cholestasis-lymphedema syndrome

ORPHA:1414Заболевание
Autosomal recessive

Cholesteryl ester storage disease

ORPHA:75234Клин. подтип
Autosomal recessive

Chondrodysplasia punctata, Toriello type

ORPHA:79347Мальформация
Autosomal recessive

Chondrodysplasia punctata, tibial-metacarpal type

ORPHA:79346Мальформация
Unknown

Chondrodysplasia with joint dislocations, gPAPP type

ORPHA:280586Мальформация
Autosomal recessive

Chondrodysplasia-difference of sex development syndrome

ORPHA:1422Мальформация
Autosomal recessive

Chondroectodermal dysplasia with night blindness

ORPHA:319195Заболевание

Chondromyxoid fibroma

ORPHA:404507Заболевание
Not applicable