Spondylo-ocular syndrome
medical condition
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Summary
Spondylo-ocular syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Spondylo-ocular syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Spondylo-ocular syndrome's instance of is recorded as rare disease[3].
- Spondylo-ocular syndrome's instance of is recorded as class of disease[4].
- Spondylo-ocular syndrome is a type of primary bone dysplasia with decreased bone density[5].
- Spondylo-ocular syndrome is a type of congenital vitreoretinal dysplasia[6].
- Spondylo-ocular syndrome is a type of syndromic cataract[7].
- Spondylo-ocular syndrome's mode of inheritance is recorded as autosomal recessive[8].
- Spondylo-ocular syndrome's health specialty is recorded as medical genetics[9].
- Spondylo-ocular syndrome's genetic association is recorded as XYLT2[10].
- Spondylo-ocular syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85194[11].