Neurology
Each bubble is a syndrome; size reflects symptom count and links connect syndromes that share symptoms. Filter by specialty and tune the overlap threshold.
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Neurology syndromes
213
Neurology
McLeod syndrome
X-linked disorder with weak Kell antigen expression, chorea and myopathy.
Neurology Medial medullary syndrome
Contralateral hemiparesis and loss of proprioception with ipsilateral tongue weakness.
Neurology MELAS syndrome
Maternally inherited stroke-like syndrome.
Neurology Meralgia paresthetica
Entrapment of the lateral femoral cutaneous nerve.
Neurology MERRF syndrome
Maternally inherited mitochondrial encephalomyopathy with myoclonus and epilepsy.
Neurology Millard–Gubler syndrome
Facial palsy with contralateral hemiparesis from a ventral pontine lesion.
Neurology Miller Fisher syndrome
Variant of Guillain–Barré syndrome with ophthalmoplegia, ataxia and areflexia.
Neurology Morvan syndrome
Autoimmune peripheral nerve hyperexcitability with encephalopathy.
Neurology Mucopolysaccharidosis type I with neurological involvement
Lysosomal storage disease with alpha-L-iduronidase deficiency.
Neurology Mucopolysaccharidosis type II with neurological involvement
X-linked lysosomal storage disease.
Neurology Mucopolysaccharidosis type III
Heparan sulfate storage with prominent neurodegeneration.
Neurology Mucopolysaccharidosis type IV with neurological involvement
Keratan sulfate storage with skeletal dysplasia.
Neurology Multiple system atrophy
Sporadic adult-onset alpha-synucleinopathy with autonomic failure and parkinsonism or cerebellar ataxia.
Neurology NARP syndrome
Maternally inherited syndrome.
Neurology Neonatal-onset multisystem inflammatory disease with neurological involvement
Cryopyrin-associated periodic syndrome with CNS involvement.
Neurology Neuro-ophthalmic autoimmune syndrome
Descriptor for immune-mediated neuro-ophthalmic disease.
Neurology Neuro-Sjögren syndrome
Neurologic involvement of Sjögren syndrome.
Neurology Neurofibromatosis type 1
Autosomal dominant neurocutaneous disorder.
Neurology Neurofibromatosis type 2
Autosomal dominant tumor predisposition.
Neurology Neuropathic pain syndrome
Pain from lesion or disease of the somatosensory nervous system.
Neurology Neurovascular compression syndrome
Cranial nerve compression by blood vessels.
Neurology Nodding syndrome
Epidemic epileptic encephalopathy in East African children.
Neurology Nothnagel syndrome
Unilateral oculomotor palsy with cerebellar ataxia.
Neurology Ohtahara syndrome
Earliest-onset developmental and epileptic encephalopathy, with tonic spasms and a suppression-burst EEG pattern.