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Browse Symptoms, Findings, Diseases & Conditions > Disease Information > Major Organs-Systems > Nervous & Sensory System (Neurology) > Disease Processes > Hereditofamilial
- 110 related diseases found
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- Disease Information
- Major Organs-Systems
- Nervous & Sensory System (Neurology)
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- Hereditofamilial
- 18p chromosome deletion complex - Disease Information
- Abdominal migraine/syndrome - Disease Information
- Acrocallosal syndrome (ACS) - Disease Information
- Alexander disease - Disease Information
- Alpha-NAGA deficency (Schindler) - Disease Information
- Amyloidosis, hereditary, neuropathic - Disease Information
- Ataxia/Oculomotor apraxia syndrome (9p13.3) - Disease Information
- Ataxia-telangiectasia - Disease Information
- Benign Familial Myoclonus - Disease Information
- Benign familial tremor - Disease Information
- Biber-Haab-Dimmer syndrome - Disease Information
- Bilateral Acoustic Neurofibromatosis (NF2) - Disease Information
- Cerebellar ataxia, congenital/hered. - Disease Information
- Cerebellar hereditofamilial degen. - Disease Information
- Cerebral AV malformation - Disease Information
- Cerebral lipidosis disorder - Disease Information
- Cervical spinal canal, shallow - Disease Information
- Chorea, chronic progressive hereditary - Disease Information
- Congenital cholinesterase deficiency - Disease Information
- Craniofacial dysostosis/Crouzon - Disease Information
- Creutzfeld-Jakob disease - Disease Information
- Curry-Jones Syndrome - Disease Information
- Dandy-Walker anomaly/syndrome - Disease Information
- Dentatorubral-Pallidoluysian Atrophy (DRPLA) - Disease Information
- Diabetes insipidus - Disease Information
- Dominant SCA/Spinal Cerebellar ataxias - Disease Information
- Duchenne's Muscular Dystrophy/Pseudohypertrophic - Disease Information
- Dysautonomia, familial - Disease Information
- Dystonia musculorum deformans - Disease Information
- Encephalomyelopathy/necro/subact/Leigh - Disease Information
- Epilepsy, myoclonic progressive fam'ial - Disease Information
- Familial cataplexy/idiopathic - Disease Information
- Familial progressive polyneuropathy - Disease Information
- Friedreich's Ataxia - Disease Information
- Gangliosidosis, generalized (GM1) - Disease Information
- Gerstmann-Straussler-Scheinker (GSS) Disease - Disease Information
- Gilles de Tourette syndrome - Disease Information
- Goldenhar syndrome - Disease Information
- Hallervorden-Spatz disease (PKAN/NBIA) - Disease Information
- Hartnup disease - Disease Information
- Hereditary autonomic/Sensory neuropathy (HSN III) - Disease Information
- Hereditary neuropathy - Disease Information
- Hereditary/neurologic degeneration synd - Disease Information
- Hermann's syndrome - Disease Information
- Huntington's chorea - Disease Information
- Hypothalamic hypogonadism, Kallman's - Disease Information
- Infantile neuroaxonal dystrophy - Disease Information
- Juvenile ceroid lipofuscinosis/Batten-M - Disease Information
- Juvenile spinal muscle atrophy (Kugelberg-Welander) - Disease Information
- Kearns-Sayre Ophthalmoplegic Syndrome - Disease Information
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