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Details of AFG3L2 gene in Homo sapiens
Phenotypes
Abnormality of central motor function, Abnormality of coordination, Abnormality of eye movement, Abnormality of higher mental function, Abnormality of movement, Abnormality of pyramidal motor function, Abnormality of saccadic eye movements, Abnormality of the central nervous system, Abnormality of the cerebellum, Abnormality of the eye, Abnormality of the hindbrain, Abnormality of the metencephalon, Abnormality of the nervous system, All, Ataxia, Autosomal dominant inheritance, Babinski sign, Cerebellar atrophy, Dysarthria, Dysmetric saccades, Gait ataxia, Gait disturbance, Gaze-evoked nystagmus, Hyperreflexia, Hypertonia, Limb ataxia, Lower limb hyperreflexia, Mode of inheritance, Morphological abnormality of the central nervous system, Neurological speech impairment, Nystagmus, Onset and clinical course, Ophthalmoparesis, Pace of progression, Phenotypic abnormality, Ptosis, Slow progression, Slow saccadic eye movements.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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