Alternative names (8)
OMIM ID • OMIM number • OMIMID • OMIMNumber • hasOMIM • hasOMIMID • hasOMIMNumber • omimIdRandom triples
| Subject | Object |
|---|---|
| gptkb:familial_progressive_hyperpigmentation | 145250 |
| gptkb:Cornelia_de_Lange_syndrome_(via_NIPBL_ortholog) | 122470 |
| gptkb:ENSG00000167552 | 182138 |
| gptkb:Loeys-Dietz_syndrome_type_1 | 609192 |
| gptkb:integrin_beta_2_(CD18) | 600065 |
| gptkb:ENSG00000026103 | 107741 |
| gptkb:PHOX2B_HUMAN | 603851 |
| gptkb:mitochondrial_intermediate_peptidase | 603868 |
| gptkb:Myelin_P0_protein | 159440 |
| gptkb:ACE2_gene | 300335 |
| gptkb:ENSG00000128313 | 182138 |
| gptkb:VEGF | 192240 (VEGFA) |
| gptkb:CREB3L1 | 609139 |
| gptkb:Mosaic_variegated_aneuploidy_syndrome | 257300 |
| gptkb:Q9UBV4 | 603377 |
| gptkb:CD80 | 112203 |
| gptkb:Reelin | 600514 |
| gptkb:Sclerosis,_Multiple | 126200 |
| gptkb:SLC25A23 | 607885 |
| gptkb:ENSG00000066468 | 146880 |