Approved symbol | SP7 |
---|---|
Approved name | Sp7 transcription factor |
HGCN ID | HGNC:17321 |
Previous symbols | |
Inheritance | |
OMIM | 606633 |
Chromosome | 12q13.13 |
Panel(s) |
NGS Mendelioom NGS Osteogenesis imperfecta en gerelateerde aandoeningen NGS Osteopetrose en gerelateerde botdysplasieën NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Skeletdysplasie |