Steel syndrome
human disease
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Steel syndrome
Summary
Steel syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Steel syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Steel syndrome's instance of is recorded as rare disease[3].
- Steel syndrome's instance of is recorded as class of disease[4].
- Steel syndrome is a type of primary bone dysplasia with defective bone mineralization[5].
- Steel syndrome's genetic association is recorded as COL27A1[6].
- Steel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_438117[7].