Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency is a rare genetic disorder caused by mutations in the CWF19L1 gene. It is characterized by progressive difficulty with balance and coordination, as well as other neurological symptoms...

Autosomal recessive cerebellar ataxia due to STUB1 deficiency is a rare genetic disorder caused by mutations in the STUB1 gene. It is characterized by progressive ataxia (lack of coordination) of the limbs and trunk, as well as intellectual disabi...

Autosomal recessive cerebellar ataxia with late-onset spasticity (ARCA-S) is a rare, inherited neurological disorder characterized by progressive ataxia (lack of muscle coordination) and spasticity (stiffness and jerky movements) that usually begi...

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency is a rare genetic disorder caused by mutations in the RUBCN gene. It is characterized by progressive cerebellar ataxia (lack of coordination), ...

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency is a rare genetic disorder caused by mutations in the TUD gene. It is characterized by progressive ataxia (lack of muscle coordination), epilepsy...

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency is a rare genetic disorder caused by mutations in the WWOX gene. It is characterized by a combination of cerebellar ataxia (a lack of coordinati...

Autosomal recessive cerebellar ataxia-movement disorder syndrome is a rare genetic disorder that affects the cerebellum, a part of the brain that controls movement. It is characterized by progressive difficulty with coordination, balance, and spee...

Autosomal recessive cerebellar ataxia-psychomotor delay syndrome (ARCPD) is a rare genetic disorder characterized by progressive ataxia (loss of coordination) and psychomotor delay (slowed development). It is caused by mutations in the SLC25A12 ge...

Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (ARCA-PNS-NAO) is a rare, inherited neurological disorder characterized by progressive ataxia (lack of muscle coordination), pyramidal signs (abnormal refl...

Autosomal recessive cerebral atrophy (ARCA) is a rare genetic disorder that affects the brain and spinal cord. It is characterized by progressive degeneration of the brain and spinal cord, leading to physical and mental disability. Symptoms may in...

Autosomal recessive Charcot-Marie-Tooth disease type 2X (AR-CMT2X) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as ...

Autosomal recessive Charcot-Marie-Tooth disease with hoarseness is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the GJB1 gene, which is responsible for the production of a protein called connexin 32. Peo...

Autosomal recessive chorioretinopathy-microcephaly syndrome (ARCM) is a rare genetic disorder characterized by a combination of eye abnormalities, including chorioretinopathy (damage to the retina) and microcephaly (abnormally small head size). Af...

Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction is a rare genetic disorder that affects the nervous system. It is caused by mutations in the KIF5A gene, which is responsible for the production of a protein called ...

Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency is a rare genetic disorder caused by mutations in the GRID2 gene. It is characterized by a lack of coordination and balance (ataxia) that is present from birth (congenital). ...

Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency is a rare genetic disorder caused by mutations in the MGLUR1 gene. This gene is responsible for the production of a protein called metabotropic glutamate receptor 1 (mGluR1)...

Autosomal recessive cutis laxa type 1 (ARCL1) is a rare genetic disorder characterized by loose, wrinkled skin, joint laxity, and a variety of other symptoms. It is caused by mutations in the ATP6V0A2 gene, which is responsible for the production ...