polymicrogyria with optic nerve hypoplasia
human disease
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polymicrogyria with optic nerve hypoplasia
Summary
polymicrogyria with optic nerve hypoplasia is a developmental defect during embryogenesis[1].
Key Facts
- polymicrogyria with optic nerve hypoplasia's instance of is recorded as developmental defect during embryogenesis[2].
- polymicrogyria with optic nerve hypoplasia's instance of is recorded as rare disease[3].
- polymicrogyria with optic nerve hypoplasia's instance of is recorded as class of disease[4].
- polymicrogyria with optic nerve hypoplasia is a type of genetic syndromic intellectual disability[5].
- polymicrogyria with optic nerve hypoplasia is a type of syndromic hereditary optic neuropathy[6].
- polymicrogyria with optic nerve hypoplasia is a type of rare genetic developmental defect during embryogenesis[7].
- polymicrogyria with optic nerve hypoplasia is a type of other syndrome with a central nervous system malformation as major feature[8].
- polymicrogyria with optic nerve hypoplasia is a type of syndromic optic nerve hypoplasia[9].
- polymicrogyria with optic nerve hypoplasia is a type of cerebral malformation with epilepsy[10].
- polymicrogyria with optic nerve hypoplasia's genetic association is recorded as TUBA8[11].
- polymicrogyria with optic nerve hypoplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_250972[12].