Tremor, mild
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant optic atrophy and cataract | (Orphanet:67036) |
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome | (Orphanet:363429) |
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency | (Orphanet:324262) |