Abduction deficits (about half of patients)
Symptom Information:
Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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OMIM: "Abduction deficits (about half of patients)" [OMIM:Abduction deficits (about half of patients)] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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2 / 7739
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Resource:
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All diseases associated with this symptom:
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome
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(Orphanet:363429)
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Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
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(Orphanet:324262)
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