MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency

ORPHA:453521Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia due to STUB1 deficiency

ORPHA:412057Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia due to a DNA repair defect

ORPHA:98097Kat.
Autosomal recessive

Autosomal recessive cerebellar ataxia with late-onset spasticity

ORPHA:352641Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome

ORPHA:404481Kl. gruppe
Autosomal recessive

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency

ORPHA:404499Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency

ORPHA:404493Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency

ORPHA:284282Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-movement disorder syndrome

ORPHA:95434Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-psychomotor delay syndrome

ORPHA:284271Kr.
Autosomal recessive

Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome

ORPHA:363429Kr.
Autosomal recessive

Autosomal recessive cerebelloparenchymal disorder type 3

ORPHA:1170Kr.
Autosomal recessive

Autosomal recessive cerebral atrophy

ORPHA:363969Kr.
Autosomal recessive

Autosomal recessive chorioretinopathy-microcephaly syndrome

ORPHA:2518Malf.
Autosomal recessive

Autosomal recessive combined immunodeficiency due to IL6R deficiency

ORPHA:656326Kr.
Autosomal recessive

Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency

ORPHA:656283Kr.
Autosomal recessive

Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency

ORPHA:656300Kr.
Autosomal recessive

Autosomal recessive complex spastic paraplegia

ORPHA:100981Kl. gruppe
Autosomal recessive

Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction

ORPHA:506353Kr.
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia

ORPHA:98095Kat.
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency

ORPHA:363432Kl. subt.
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency

ORPHA:324262Kl. subt.
Autosomal recessive

Autosomal recessive congenital ichthyosis

ORPHA:281097Kl. gruppe
Autosomal recessive

Autosomal recessive congenital myasthenic syndrome due to defective synaptic vesicles exocytosis

ORPHA:716903Ätl. subt.
Autosomal recessive