| Disease Browser
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Parent Node:
 neurodegenerative disease (MONDO:0005559) |
..Starting node
.. inherited neurodegenerative disorder ()
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Child Nodes:
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| ........adult spinal muscular atrophy () |
| ........Alexander disease () |
| ........angioid streaks of choroid () |
| ........attenuated ChC)diak-Higashi syndrome () |
| ........autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures () |
| ........autosomal recessive cerebral atrophy () |
| ........boylan dew greco syndrome () |
| ........Canavan disease () |
| ........Chediak-Higashi syndrome () |
| ........Cockayne syndrome () |
........deafness dystonia syndrome ()  L: 00113; |
| ........dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities () |
| ........early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome () |
| ........encephalopathy due to beta-mercaptolactate-cysteine disulfiduria () |
| ........facial onset sensory and motor neuronopathy () |
| ........familial amyotrophic lateral sclerosis () |
| ........familial infantile bilateral striatal necrosis () L: 00075; |
| ........fatal post-viral neurodegenerative disorder () |
| ........ferro-cerebro-cutaneous syndrome () |
| ........genetic neurodegenerative disease with dementia () |
| ........GM2 gangliosidosis () |
| ........hereditary optic atrophy () |
| ........hereditary spastic paraplegia () |
| ........Huntington disease and related disorders () |
| ........hypotonia-speech impairment-severe cognitive delay syndrome () |
| ........infantile cerebellar-retinal degeneration () L: 00108; |
| ........infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome () |
| ........intermediate spinal muscular atrophy () |
| ........ITPA-related encephalopathy () |
| ........juvenile spinal muscular atrophy () |
| ........Krabbe disease () |
| ........lateral sclerosis () |
| ........leukoencephalopathy-metaphyseal chondrodysplasia syndrome () |
| ........microphthalmia-brain atrophy syndrome () |
| ........mitochondrial DNA depletion syndrome 4a () L: 00032; |
| ........multiple mitochondrial dysfunctions syndrome 4 () L: 00530; |
| ........multiple sclerosis, susceptibility to, 2 () |
| ........multiple sclerosis, susceptibility to, 3 () |
| ........multiple sclerosis, susceptibility to, 4 () |
| ........muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome () |
| ........myoclonic cerebellar dyssynergia () |
| ........neurodegenerative syndrome due to cerebral folate transport deficiency () |
| ........neuronal ceroid lipofuscinosis () |
| ........neuronal intranuclear inclusion disease () |
| ........neuronopathy, distal hereditary motor, type 2A () |
| ........neuronopathy, distal hereditary motor, type 7A () |
| ........Parkinson disease 18, autosomal dominant, susceptibility to () |
| ........Parkinson disease 5, autosomal dominant, susceptibility to () |
| ........PEHO syndrome () |
| ........Pelizaeus-Merzbacher disease () |
| ........posterior cortical atrophy () |
| ........psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome () |
| ........radiation sensitivity/chromosome instability syndrome, autosomal dominant () |
| ........recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome () |
| ........severe neurodegenerative syndrome with lipodystrophy () |
| ........striatonigral degeneration, childhood-onset () |
| ........tuberous sclerosis () |
| ........vitreoretinal degeneration () |
| ........X-linked adrenoleukodystrophy () |
| ........X-linked neurodegenerative syndrome, Bertini type () |
| ........X-linked neurodegenerative syndrome, Hamel type () |
Sister Nodes: |
..amyotrophic lateral sclerosis ()
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..brachial amyotrophic diplegia ()
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..cerebellar degeneration ()
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..cerebral degeneration ()
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..corticobasal degeneration disorder ()
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..demyelinating disease ()
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..eye degenerative disease ()
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..inherited neurodegenerative disorder ()
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..Marchiafava-Bignami disease ()
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..neuroaxonal dystrophy ()
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..neurodegenerative disease with chorea ()
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..neurodegenerative disease with dementia ()
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..olivopontocerebellar atrophy ()
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..optic atrophy ()
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..primary progressive apraxia of speech ()
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..secondary Parkinson disease ()
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..senile degeneration of brain ()
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..synucleinopathy ()
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..tauopathy ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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