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(HPO:0002066) | Gait ataxia | Frequent [Orphanet] | 327 / 7739 | |||
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(HPO:0100022) | Abnormality of movement | Very frequent [Orphanet] | 129 / 7739 | |||
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(HPO:0002588) | Duodenal ulcer | 15 / 7739 | ||||
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(HPO:0002592) | Gastric ulcer | Very frequent [Orphanet] | 39 / 7739 | |||
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(HPO:0000639) | Nystagmus | Very frequent [Orphanet] | 555 / 7739 | |||
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(HPO:0001317) | Abnormality of the cerebellum | 36 / 7739 | ||||
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(HPO:0001337) | Tremor | 200 / 7739 | ||||
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(MedDRA:10015496) | Essential tremor | 4 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |