All terms in OMIM

Label Id Description
SERGEF 606051
congenital disorder of glycosylation, type iib 606056
Congenital disorders of glycosylation, type II PS212066
RAPGEF3 606057
propionic acidemia 606054
PCTP 606055
familial adenomatous polyposis 1 175100
Familial adenomatous polyposis PS175100
RAPGEF4 606058
PKIA 606059
GCK 138079
teeth, odd shapes of 187000
triphalangeal thumbs and dislocation of patella 190650
dystonia 2, torsion, autosomal recessive 224500
Dystonia PS128100
ossicular malformations, familial 165680
CCL5 187011
187010 187010
H6PD 138090
175000 175000