All terms in OMIM

Label Id Description
invasion inhibitory protein, 45-kd 608772
HBA2 141850
LYNX1 606110
MED13L 608771
RPP30 606115
KLHL10 608778
POSTN 608777
RPP38 606116
congenital disorder of glycosylation, type il 608776
Congenital disorders of glycosylation, type I PS212065
POP7 606113
POP4 606114
HAUS1 608775
CYGB 608759
cardiomyopathy, familial hypertrophic, 10 608758
CLP1 608757
GPT2 138210
phosphoenolpyruvate carboxykinase deficiency, cytosolic 261680
101101770 101101770
macular dystrophy, vitelliform, 1 153840