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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Childhood-onset benign chorea with striatal involvement

ORPHA:494541Disease
Autosomal dominant

Childhood-onset common variable immunodeficiency due to ARHGEF1 deficiency

ORPHA:696942Disease
Autosomal recessive

Childhood-onset hypophosphatasia

ORPHA:247667Clin. sub.
Autosomal dominant, Autosomal recessive

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

ORPHA:500180Disease
Autosomal dominant

Childhood-onset nemaline myopathy

ORPHA:171439Disease
Autosomal dominant

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

ORPHA:466921Disease
Autosomal recessive

Childhood-onset schizophrenia

ORPHA:641496Disease

Childhood-onset spasticity with hyperglycinemia

ORPHA:401866Disease
Autosomal recessive

Childhood-onset stress-induced neurodegenerative ataxia-seizure syndrome

ORPHA:694922Disease
Autosomal recessive

Choanal atresia

ORPHA:137914Morph.
Not applicable

Choanal atresia, bilateral

ORPHA:137920Clin. sub.
Not applicable

Choanal atresia, unilateral

ORPHA:137917Clin. sub.
Not applicable

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

ORPHA:589856Malform.
Autosomal dominant

Cholangiocarcinoma

ORPHA:70567Disease
Not applicable

Choledochal cyst

ORPHA:480501Morph.

Cholera

ORPHA:173Disease
Not applicable

Cholestasis-lymphedema syndrome

ORPHA:1414Disease
Autosomal recessive

Cholesteryl ester storage disease

ORPHA:75234Clin. sub.
Autosomal recessive

Chondrodysplasia punctata, Toriello type

ORPHA:79347Malform.
Autosomal recessive

Chondrodysplasia punctata, tibial-metacarpal type

ORPHA:79346Malform.
Unknown

Chondrodysplasia with joint dislocations, gPAPP type

ORPHA:280586Malform.
Autosomal recessive

Chondrodysplasia-difference of sex development syndrome

ORPHA:1422Malform.
Autosomal recessive

Chondroectodermal dysplasia with night blindness

ORPHA:319195Disease

Chondromyxoid fibroma

ORPHA:404507Disease
Not applicable