Wikidata entity: Q6839894
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2293 | genetic association | ... | Q17909078 (COX7B) | COX7B |
| P2293 | genetic association | ... | Q18026830 (HCCS) | HCCS |
| P2293 | genetic association | ... | Q18041082 (NDUFB11) | NDUFB11 |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P279 | subclass of | ... | Q179630 (syndrome) | syndrome |
| P279 | subclass of | ... | Q29982037 (syndromic microphthalmia) | syndromic microphthalmia |
| P699 | Disease Ontology ID | DOID:0111875 |
| P4317 | GARD rare disease ID | 3659 |
| P668 | GeneReviews ID | NBK7041 |
| P7464 | Genetics Home Reference Conditions ID | microphthalmia-with-linear-skin-defects-syndrome |
| P7807 | ICD-11 ID (Foundation) | 526014677 |
| P665 | KEGG ID | H01904 |
| P6366 | Microsoft Academic ID (discontinued) | 2780228798 |
| P492 | OMIM ID | 309801 |
| P492 | OMIM ID | 309801 |
| P1550 | Orphanet ID | 2556 |
| P2892 | UMLS CUI | C0796070 |
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log id: 6536923