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's subclass of is recorded as neuronal migration disorder[5].
- occipital pachygyria and polymicrogyria's subclass of is recorded as Pachygyria[6].
- occipital pachygyria and polymicrogyria's subclass of is recorded as polymicrogyria[7].
- occipital pachygyria and polymicrogyria's OMIM ID is recorded as 614115[8].
- occipital pachygyria and polymicrogyria's Orphanet ID is recorded as 280640[9].
- occipital pachygyria and polymicrogyria's genetic association is recorded as LAMC3[10].
- occipital pachygyria and polymicrogyria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_280640[11].
- occipital pachygyria and polymicrogyria's UMLS CUI is recorded as C3279875[12].
- occipital pachygyria and polymicrogyria's UMLS CUI is recorded as C5190688[13].
- occipital pachygyria and polymicrogyria's ICD-10-CM is recorded as Q04.3[14].
- occipital pachygyria and polymicrogyria's Mondo ID is recorded as MONDO_0013583[15].
- occipital pachygyria and polymicrogyria's UniProt disease ID is recorded as DI-03207[16].