MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Juvenile dermatomyositis

ORPHA:93672Kr.
Not applicable

Juvenile glaucoma

ORPHA:98977Kr.
Autosomal dominant

Juvenile hyaline fibromatosis

ORPHA:2028Kl. subt.
Autosomal recessive

Juvenile idiopathic arthritis

ORPHA:92Kl. gruppe

Juvenile myasthenia gravis

ORPHA:391497Kl. subt.
Not applicable

Juvenile myelomonocytic leukemia

ORPHA:86834Kr.
Not applicable

Juvenile myoclonic epilepsy

ORPHA:307Kr.
Multigenic/multifactorial

Juvenile nasopharyngeal angiofibroma

ORPHA:289596Kr.
Not applicable

Juvenile nephronophthisis

ORPHA:93592Kl. subt.
Autosomal recessive

Juvenile nephropathic cystinosis

ORPHA:411634Kl. subt.
Autosomal recessive

Juvenile or adult CACH syndrome

ORPHA:157719Kl. subt.
Autosomal recessive

Juvenile overlap myositis

ORPHA:329894Kr.

Juvenile polymyositis

ORPHA:93568Kr.

Juvenile polyposis of infancy

ORPHA:79076Kl. subt.
Autosomal dominant, Not applicable

Juvenile polyposis syndrome

ORPHA:2929Kr.
Autosomal dominant

Juvenile primary lateral sclerosis

ORPHA:247604Kr.
Autosomal recessive

Juvenile sialidosis type 2

ORPHA:93399Kl. subt.
Autosomal recessive

Juvenile temporal arteritis

ORPHA:26137Kr.
Unknown

Juvenile xanthogranuloma

ORPHA:158000Kr.
Not applicable

Juvenile-onset Steinert myotonic dystrophy

ORPHA:589827Kl. subt.
Autosomal dominant

Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome

ORPHA:445062Kr.
Autosomal recessive

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

ORPHA:457193Malf.
Autosomal dominant

KBG syndrome

ORPHA:2332Malf.
Autosomal dominant

KCNQ2-related developmental and epileptic encephalopathy

ORPHA:439218Kr.
Autosomal dominant