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's subclass of is recorded as primary bone dysplasia with defective bone mineralization[5].
- Steel syndrome's OMIM ID is recorded as 615155[6].
- Steel syndrome's KEGG ID is recorded as H02300[7].
- Steel syndrome's Orphanet ID is recorded as 438117[8].
- Steel syndrome's genetic association is recorded as COL27A1[9].
- Steel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_438117[10].
- Steel syndrome's UMLS CUI is recorded as C3554594[11].
- Steel syndrome's ICD-10-CM is recorded as Q87.5[12].
- Steel syndrome's Mondo ID is recorded as MONDO_0014061[13].
- Steel syndrome's UniProt disease ID is recorded as DI-04187[14].