Agenesis of the cingulate gyrus
Symptom Information:
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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: "Agenesis of the cingulate gyrus" [OMIM:Agenesis of the cingulate gyrus] |
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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:
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Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
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(Orphanet:137681)
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Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency
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(Orphanet:88639)
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