Medicine & Life Sciences
Phenotype
100%
Cerebellar Ataxia
96%
Ataxia
95%
Spastic Ataxia
84%
Paraplegia
80%
Spinocerebellar Ataxia 12
68%
Spinocerebellar Ataxia 17
65%
Genes
64%
Alexander Disease
57%
lamin B1
57%
Polynucleotide 5'-Hydroxyl-Kinase
53%
Mutation
52%
tributyl phosphate
52%
polyglutamine
45%
Dysphonia
44%
Microcephaly
42%
Penetrance
39%
Nuclear Envelope
39%
Nuclear Proteins
35%
Phosphoric Monoester Hydrolases
35%
Craniocerebral Trauma
34%
Leukoencephalopathies
30%
Marinesco-Sjogren-like syndrome (MSLS)
27%
Dystonia
27%
Neurologic Gait Disorders
25%
Alleles
25%
Tremor
24%
Spinocerebellar Ataxias
23%
Hereditary Spastic Paraplegia
22%
White Matter
17%
Glucosylceramidase
16%
Neuroimaging
15%
Corpus Callosum
15%
High-Throughput Nucleotide Sequencing
14%
Seizures
13%
Scoliosis
12%
Motor Neurons
12%
Cataract
10%
Upper Extremity
10%
Oculodentodigital Dysplasia
10%
Disease Progression
10%
Peroxisome biogenesis disorders
10%
Diffusion Tensor Imaging
9%
Magnetic Resonance Imaging
9%
Natural History
9%
Quebec
9%
Premature Mortality
8%
Differential Diagnosis
8%
Cognitive Dysfunction
8%
Age of Onset
7%
Arts & Humanities
Phenotype
39%
Corpus Callosum
19%
Gene
18%
Mutation
10%
Lesion
9%
Cohort
7%
Onset
6%