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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Juvenile dermatomyositis

ORPHA:93672Disease
Not applicable

Juvenile glaucoma

ORPHA:98977Disease
Autosomal dominant

Juvenile hyaline fibromatosis

ORPHA:2028Clin. sub.
Autosomal recessive

Juvenile idiopathic arthritis

ORPHA:92Clin. grp.

Juvenile myasthenia gravis

ORPHA:391497Clin. sub.
Not applicable

Juvenile myelomonocytic leukemia

ORPHA:86834Disease
Not applicable

Juvenile myoclonic epilepsy

ORPHA:307Disease
Multigenic/multifactorial

Juvenile nasopharyngeal angiofibroma

ORPHA:289596Disease
Not applicable

Juvenile nephronophthisis

ORPHA:93592Clin. sub.
Autosomal recessive

Juvenile nephropathic cystinosis

ORPHA:411634Clin. sub.
Autosomal recessive

Juvenile or adult CACH syndrome

ORPHA:157719Clin. sub.
Autosomal recessive

Juvenile overlap myositis

ORPHA:329894Disease

Juvenile polymyositis

ORPHA:93568Disease

Juvenile polyposis of infancy

ORPHA:79076Clin. sub.
Autosomal dominant, Not applicable

Juvenile polyposis syndrome

ORPHA:2929Disease
Autosomal dominant

Juvenile primary lateral sclerosis

ORPHA:247604Disease
Autosomal recessive

Juvenile sialidosis type 2

ORPHA:93399Clin. sub.
Autosomal recessive

Juvenile temporal arteritis

ORPHA:26137Disease
Unknown

Juvenile xanthogranuloma

ORPHA:158000Disease
Not applicable

Juvenile-onset Steinert myotonic dystrophy

ORPHA:589827Clin. sub.
Autosomal dominant

Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome

ORPHA:445062Disease
Autosomal recessive

KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome

ORPHA:457193Malform.
Autosomal dominant

KBG syndrome

ORPHA:2332Malform.
Autosomal dominant

KCNQ2-related developmental and epileptic encephalopathy

ORPHA:439218Disease
Autosomal dominant