Alternative names (8)
OMIM ID • OMIM number • OMIMID • OMIMNumber • hasOMIM • hasOMIMID • hasOMIMNumber • omimIdRandom triples
| Subject | Object |
|---|---|
| gptkb:ENSG00000164754 | 138190 |
| gptkb:familial_chylomicronemia_syndrome | 238600 |
| gptkb:IL6R | 147880 |
| gptkb:NKX2-5_cardiac_homeobox | 600584 |
| gptkb:Caspase-1 | 147678 |
| gptkb:Toll-like_receptor_5 | 603599 |
| gptkb:BAT1_gene | 601238 |
| gptkb:MGI:96433 | 191170 |
| gptkb:Fanconi_anemia,_complementation_group_D2 | 227646 |
| gptkb:Gerstmann–Sträussler–Scheinker_syndrome | 137440 |
| gptkb:RECQL4 | 603780 |
| gptkb:Glutamate_decarboxylase_65 | 138275 |
| gptkb:WNT4_gene | 603490 |
| gptkb:chromosome_Y | 400000 |
| gptkb:WNT8A_gene | 606360 |
| gptkb:NEIL1 | 608844 |
| gptkb:MAPK9 | 602448 |
| gptkb:Andersen_disease | 232500 |
| gptkb:familial_combined_hyperlipidemia | 144250 |
| gptkb:ENSG00000188536 | 138190 |