Alternative names (8)
OMIM ID • OMIM number • OMIMID • OMIMNumber • hasOMIM • hasOMIMID • hasOMIMNumber • omimIdRandom triples
| Subject | Object |
|---|---|
| gptkb:WNT1 | 164820 |
| gptkb:SURF91 | 185620 |
| gptkb:platelet-derived_growth_factor_receptor_alpha | 173490 |
| gptkb:hemoglobin_H_disease | 141800 |
| gptkb:hypereosinophilic_syndrome | 606800 |
| gptkb:oculocutaneous_albinism_type_4 | 606574 |
| gptkb:CLTA | 118955 |
| gptkb:ENSG00000157764 | 164757 |
| gptkb:ADRB1 | 109630 |
| gptkb:ENSG00000104312 | 188410 |
| gptkb:BMPR2 | 600799 |
| gptkb:TREM2 | 605086 |
| gptkb:ENSG00000136868 | 600185 |
| gptkb:Retinoblastoma_protein_(RB1) | 614041 |
| gptkb:ABC_transporters | 601107 |
| gptkb:RA-GEF-2 | 605370 |
| gptkb:Meniere's_Disease | 156000 |
| gptkb:collagen_XV | 120328 |
| gptkb:PTX1_gene | 602492 |
| gptkb:Wilson_disease | 277900 |