familial cavitary optic disc anomaly
human disease
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Summary
familial cavitary optic disc anomaly is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- familial cavitary optic disc anomaly's instance of is recorded as developmental defect during embryogenesis[3].
- familial cavitary optic disc anomaly's instance of is recorded as rare disease[4].
- familial cavitary optic disc anomaly's instance of is recorded as class of disease[5].
- familial cavitary optic disc anomaly is a type of rare eye disease due to a differentiation anomaly[6].
- familial cavitary optic disc anomaly's genetic association is recorded as MMP19[7].
- familial cavitary optic disc anomaly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_464760[8].
Why It Matters
familial cavitary optic disc anomaly is known by 5 alternative names across languages and contexts.[2]