Approved symbol | PITPNM3 |
---|---|
Approved name | PITPNM family member 3 |
HGCN ID | HGNC:21043 |
Previous symbols | CORD5 |
Inheritance | |
OMIM | 608921 |
Chromosome | 17p13.2-p13.1 |
Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |