MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency

ORPHA:453521Disease
Autosomal recessive

Autosomal recessive cerebellar ataxia due to STUB1 deficiency

ORPHA:412057Disease
Autosomal recessive

Autosomal recessive cerebellar ataxia due to a DNA repair defect

ORPHA:98097Cat.
Autosomal recessive

Autosomal recessive cerebellar ataxia with late-onset spasticity

ORPHA:352641Disease
Autosomal recessive

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome

ORPHA:404481Clin. grp.
Autosomal recessive

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

ORPHA:404499Disease
Autosomal recessive

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

ORPHA:404493Disease
Autosomal recessive

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

ORPHA:284282Disease
Autosomal recessive

Autosomal recessive cerebellar ataxia-movement disorder syndrome

ORPHA:95434Disease
Autosomal recessive

Autosomal recessive cerebellar ataxia-psychomotor delay syndrome

ORPHA:284271Disease
Autosomal recessive

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

ORPHA:363429Disease
Autosomal recessive

Autosomal recessive cerebelloparenchymal disorder type 3

ORPHA:1170Disease
Autosomal recessive

Autosomal recessive cerebral atrophy

ORPHA:363969Disease
Autosomal recessive

Autosomal recessive chorioretinopathy-microcephaly syndrome

ORPHA:2518Malform.
Autosomal recessive

Autosomal recessive combined immunodeficiency due to IL6R deficiency

ORPHA:656326Disease
Autosomal recessive

Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency

ORPHA:656283Disease
Autosomal recessive

Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency

ORPHA:656300Disease
Autosomal recessive

Autosomal recessive complex spastic paraplegia

ORPHA:100981Clin. grp.
Autosomal recessive

Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction

ORPHA:506353Disease
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia

ORPHA:98095Cat.
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency

ORPHA:363432Clin. sub.
Autosomal recessive

Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency

ORPHA:324262Clin. sub.
Autosomal recessive

Autosomal recessive congenital ichthyosis

ORPHA:281097Clin. grp.
Autosomal recessive

Autosomal recessive congenital myasthenic syndrome due to defective synaptic vesicles exocytosis

ORPHA:716903Etio. sub.
Autosomal recessive