Autosomal dominant Charcot-Marie-Tooth disease type 2O (CMT2O) 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 sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2Q (CMT2Q) is a rare inherited neurological disorder that affects the peripheral nerves. It is caused by mutations in the GARS gene, which is responsible for the production of the protein glycine...

Autosomal dominant Charcot-Marie-Tooth disease type 2U (CMT2U) 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 sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2V (CMT2V) 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 sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2W (CMT2W) 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 sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2Y (CMT2Y) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by slowly progressive muscle weakness and wasting in the lower legs, feet, and hands, ...

Autosomal dominant Charcot-Marie-Tooth disease type 2Z (CMT2Z) 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 sens...

Autosomal dominant coarctation of aorta is a genetic disorder that affects the aorta, the main artery that carries blood from the heart to the rest of the body. It is caused by a narrowing of the aorta, which can lead to high blood pressure, heart...

Autosomal dominant congenital benign spinal muscular atrophy (ADCBSMA) is a rare genetic disorder that affects the muscles of the spine and lower body. It is caused by a mutation in the SMN1 gene, which is responsible for producing a protein that ...

Autosomal dominant cutis laxa is a rare genetic disorder that affects the skin. It is characterized by loose, wrinkled skin that is prone to sagging and stretching. It is caused by mutations in the elastin gene, which is responsible for producing ...

Autosomal dominant deafness-onychodystrophy syndrome (ADOD) is a rare genetic disorder characterized by hearing loss, nail abnormalities, and skin changes. It is caused by mutations in the GJB2 gene, which is responsible for the production of a pr...

Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome (AD-MNM) is a rare genetic disorder characterized by progressive muscle weakness and wasting (atrophy) of the lower limbs, as well as sensory disturbances in the feet...

Autosomal dominant distal renal tubular acidosis (dRTA) is a rare inherited disorder that affects the kidneys' ability to regulate acid-base balance in the body. It is caused by a mutation in the SLC4A1 gene, which is responsible for the productio...

Autosomal dominant dopa-responsive dystonia (DRD) is a rare inherited neurological disorder that is characterized by dystonia, a movement disorder that causes involuntary muscle contractions and abnormal postures. It is caused by a mutation in the...

Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) is a rare genetic disorder that affects the muscles and connective tissues. It is caused by a mutation in the gene that codes for the protein emerin, which is found in the inner membrane ...

Autosomal dominant epidermolytic ichthyosis (ADEI) is a rare genetic skin disorder that is characterized by thick, scaly skin. It is caused by a mutation in the keratin gene, which is responsible for the production of proteins that make up the ski...