All terms in OMIM

Label Id Description
SIGLEC14 618132
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 8 618135
Muscular dystrophy, limb-girdle, autosomal recessive PS253600
Muscular dystrophy-dystroglycanopathy, type C PS609308
UTS2B 618134
mis18 kinetochore protein a: mis18a 618137
MAD2L1BP 618136
MIS18BP1 618139
muscular dystrophy, limb-girdle, autosomal recessive 23 618138
muscular dystrophy, limb-girdle, autosomal dominant 4 618129
Muscular dystrophy, limb-girdle, autosomal dominant PS603511
BBS2 606151
SLC19A3 606152
FADS3 606150
von willebrand disease, platelet-type 177820
Bleeding disorder, platelet-type PS231200
platyspondylic lethal skeletal dysplasia, torrance type 151210
606155 606155
retinitis pigmentosa 91 153870
GRINA 138251