Wikidata entity: Q1760294
| P373 | Commons category | String | Trigonocephaly | ??? |
| P1889 | different from | ... | Q132775626 (metopic ridge) | metopic ridge |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q14914258 (FGFR1) | FGFR1 |
| P2293 | genetic association | ... | Q18052392 (FREM1) | FREM1 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q12136 (disease) | disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P279 | subclass of | ... | Q378183 (craniosynostosis) | craniosynostosis |
| P557 | DiseasesDB | 33252 |
| P1417 | Encyclopædia Britannica Online ID | science/trigonocephaly |
| P646 | Freebase ID | /m/01hrgg |
| P494 | ICD-10 ID | Q75.0 |
| P7807 | ICD-11 ID (Foundation) | 20816218 |
| P493 | ICD-9 ID | 756.0 |
| P665 | KEGG ID | H01207 |
| P6366 | Microsoft Academic ID (discontinued) | 2778888786 |
| P5270 | Mondo ID | MONDO_0013774 |
| P492 | OMIM ID | 190440 |
| P492 | OMIM ID | 190440 |
| P492 | OMIM ID | 614485 |
| P492 | OMIM ID | 614485 |
| P10283 | OpenAlex ID | C2778888786 |
| P2892 | UMLS CUI | C3280974 |
| P11143 | WikiProjectMed ID | Trigonocephaly |
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