Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia

Nume		Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Cerebellar ataxia with defective DNA repair; Early-onset cerebellar ataxia
Clasificare anatomică Malacards		Boli ale ochiului; Boli neuronale

Boli A-Z		Aceruloplasminemia Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Analbuminemia Aniridia 1 Anorexia Nervosa 1 Apraxia Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Ataxia with Vitamin E Deficiency Autosomal Recessive Cerebellar Ataxia Axonal Neuropathy Blood Group--Ahonen Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes Cerebellar Disease Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Dystonia Friedreich Ataxia 1 Hepatic Adenomas, Familial Hereditary Ataxia Hinman Syndrome Hypercholesterolemia, Autosomal Dominant, 3 Neuropathy Ocular Motor Apraxia Refsum Disease, Classic Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spinocerebellar Ataxia 31 Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Ataxia with Axonal Neuropathy Type 2 Spondyloocular Syndrome Tetraamelia Syndrome, Autosomal Recessive Vitamin E, Familial Isolated Deficiency of