Gene: [0Xq2/OPD1] otopalatodigital syndrome 1; [OPD ]
|
HET |
The GEM and MIM catalogues indicate two X-linked variants of OPD syndrome; see GEM:0X^/OPD2." |
|
HIS |
HGM considers only one OPD locus as being mapped, HGM9.5 indicating OPD/31130 and HGM10 indicating OPD/30412; without comments on these discrepancies." |
|
REF |
PHE,FOG,PAT "Dudding &: Am J Dis Child, 113, 214-221, 1967 PHE,FOG,PAT "Gall &: AJHG, 24, 24-36, 1972 PHE,FOG,PAT "Langer: Am J Roentgenol, 100, 63-70, 1967 PHE,FOG,PAT "Pazzaglia, Beluffi: Clin Genet, 30, 338-344, 1986 HIS,PHE,LOC,LIN "Weinstein, Cohen: J Med Genet, 3, 17-22, 1966 |
|
KEY |
devd, bone |
|
CLA |
unknown, basic |
|
LOC |
0X q26-28 |
|
MIM |
MIM: 311300 |
|
SYN |
OPD |
