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's subclass of is recorded as genetic syndromic intellectual disability^[5].
• polymicrogyria with optic nerve hypoplasia's subclass of is recorded as syndromic hereditary optic neuropathy^[6].
• polymicrogyria with optic nerve hypoplasia's subclass of is recorded as rare genetic developmental defect during embryogenesis^[7].
• polymicrogyria with optic nerve hypoplasia's subclass of is recorded as other syndrome with a central nervous system malformation as major feature^[8].
• polymicrogyria with optic nerve hypoplasia's subclass of is recorded as syndromic optic nerve hypoplasia^[9].
• polymicrogyria with optic nerve hypoplasia's subclass of is recorded as cerebral malformation with epilepsy^[10].
• polymicrogyria with optic nerve hypoplasia's MeSH descriptor ID is recorded as C567715^[11].
• polymicrogyria with optic nerve hypoplasia's OMIM ID is recorded as 613180^[12].
• polymicrogyria with optic nerve hypoplasia's Orphanet ID is recorded as 250972^[13].
• polymicrogyria with optic nerve hypoplasia's genetic association is recorded as TUBA8^[14].
• polymicrogyria with optic nerve hypoplasia's Google Knowledge Graph ID is recorded as /g/11g_zyxq_g^[15].
• polymicrogyria with optic nerve hypoplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_250972^[16].
• polymicrogyria with optic nerve hypoplasia's UMLS CUI is recorded as C2750798^[17].
• polymicrogyria with optic nerve hypoplasia's Mondo ID is recorded as MONDO_0013172^[18].