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