occipital pachygyria and polymicrogyria
human disease
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occipital pachygyria and polymicrogyria
Summary
occipital pachygyria and polymicrogyria is a developmental defect during embryogenesis[1].
Key Facts
- occipital pachygyria and polymicrogyria's instance of is recorded as developmental defect during embryogenesis[2].
- occipital pachygyria and polymicrogyria's instance of is recorded as rare disease[3].
- occipital pachygyria and polymicrogyria's instance of is recorded as class of disease[4].
- occipital pachygyria and polymicrogyria is a type of neuronal migration disorder[5].
- occipital pachygyria and polymicrogyria is a type of Pachygyria[6].
- occipital pachygyria and polymicrogyria is a type of polymicrogyria[7].
- occipital pachygyria and polymicrogyria's genetic association is recorded as LAMC3[8].
- occipital pachygyria and polymicrogyria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_280640[9].