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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Juvenile dermatomyositis

ORPHA:93672Ауру
Not applicable

Juvenile glaucoma

ORPHA:98977Ауру
Autosomal dominant

Juvenile hyaline fibromatosis

ORPHA:2028Клин. под.
Autosomal recessive

Juvenile idiopathic arthritis

ORPHA:92Клин. топ

Juvenile myasthenia gravis

ORPHA:391497Клин. под.
Not applicable

Juvenile myelomonocytic leukemia

ORPHA:86834Ауру
Not applicable

Juvenile myoclonic epilepsy

ORPHA:307Ауру
Multigenic/multifactorial

Juvenile nasopharyngeal angiofibroma

ORPHA:289596Ауру
Not applicable

Juvenile nephronophthisis

ORPHA:93592Клин. под.
Autosomal recessive

Juvenile nephropathic cystinosis

ORPHA:411634Клин. под.
Autosomal recessive

Juvenile or adult CACH syndrome

ORPHA:157719Клин. под.
Autosomal recessive

Juvenile overlap myositis

ORPHA:329894Ауру

Juvenile polymyositis

ORPHA:93568Ауру

Juvenile polyposis of infancy

ORPHA:79076Клин. под.
Autosomal dominant, Not applicable

Juvenile polyposis syndrome

ORPHA:2929Ауру
Autosomal dominant

Juvenile primary lateral sclerosis

ORPHA:247604Ауру
Autosomal recessive

Juvenile sialidosis type 2

ORPHA:93399Клин. под.
Autosomal recessive

Juvenile temporal arteritis

ORPHA:26137Ауру
Unknown

Juvenile xanthogranuloma

ORPHA:158000Ауру
Not applicable

Juvenile-onset Steinert myotonic dystrophy

ORPHA:589827Клин. под.
Autosomal dominant

Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome

ORPHA:445062Ауру
Autosomal recessive

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

ORPHA:457193Мальф.
Autosomal dominant

KBG syndrome

ORPHA:2332Мальф.
Autosomal dominant

KCNQ2-related developmental and epileptic encephalopathy

ORPHA:439218Ауру
Autosomal dominant