Wikidata entity: Q378183

Quantities
| P1193 | prevalence | 0.000045 |
| P373 | Commons category | String | Craniosynostosis | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q18031873 (TCF12) | TCF12 |
| P2293 | genetic association | ... | Q18038733 (BBS9) | BBS9 |
| P2293 | genetic association | ... | Q14906427 (TWIST1) | TWIST1 |
| P2293 | genetic association | ... | Q14911644 (FGFR2) | FGFR2 |
| P2293 | genetic association | ... | Q14913261 (SKI) | SKI |
| P2293 | genetic association | ... | Q17917473 (ERF) | ERF |
| P2293 | genetic association | ... | Q18029465 (MSX2) | MSX2 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P667 | ICPC 2 ID | String | L82 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C84655 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q929833 (rare disease) | rare disease |
| P279 | subclass of | ... | Q2141048 (synostosis) | synostosis |
| P279 | subclass of | ... | Q5182134 (craniofacial disease) | craniofacial disease |
| P508 | BNCF Thesaurus ID | 25566 |
| P699 | Disease Ontology ID | DOID:2340 |
| P557 | DiseasesDB | 3160 |
| P4746 | Elhuyar ZTH ID | 027011 |
| P673 | eMedicine ID | 248568 |
| P10565 | Encyclopedia of China (Third Edition) ID | 464605 |
| P1417 | Encyclopædia Britannica Online ID | science/craniosynostosis |
| P3219 | Encyclopædia Universalis ID | craniosynostoses |
| P646 | Freebase ID | /m/05dbhj |
| P4317 | GARD rare disease ID | 6209 |
| P668 | GeneReviews ID | NBK1455 |
| P3841 | Human Phenotype Ontology ID | HP:0000262 |
| P3841 | Human Phenotype Ontology ID | HP:0001363 |
| P3841 | Human Phenotype Ontology ID | HP:0000263 |
| P3841 | Human Phenotype Ontology ID | HP:0000243 |
| P4229 | ICD-10-CM | Q75.0 |
| P7807 | ICD-11 ID (Foundation) | 458033798 |
| P7329 | ICD-11 ID (MMS) | LB70.0 |
| P3827 | JSTOR topic ID (archived) | craniosynostoses |
| P8408 | KBpedia ID | Craniosynostosis |
| P665 | KEGG ID | H00458 |
| P604 | MedlinePlus ID | 001590 |
| P604 | MedlinePlus ID | 001590 |
| P486 | MeSH descriptor ID | D003398 |
| P672 | MeSH tree code | C05.116.099.370.894.232 |
| P672 | MeSH tree code | C05.660.207.240 |
| P672 | MeSH tree code | C05.660.906.364 |
| P672 | MeSH tree code | C16.131.621.207.240 |
| P672 | MeSH tree code | C16.131.621.906.364 |
| P6366 | Microsoft Academic ID (discontinued) | 2909233398 |
| P5270 | Mondo ID | MONDO_0015469 |
| P7995 | NHS Health A to Z ID | craniosynostosis |
| P492 | OMIM ID | 615314 |
| P492 | OMIM ID | 615314 |
| P492 | OMIM ID | 123100 |
| P492 | OMIM ID | 123100 |
| P492 | OMIM ID | 182212 |
| P492 | OMIM ID | 182212 |
| P492 | OMIM ID | 604757 |
| P492 | OMIM ID | 604757 |
| P492 | OMIM ID | 600775 |
| P492 | OMIM ID | 600775 |
| P492 | OMIM ID | 600593 |
| P492 | OMIM ID | 600593 |
| P10283 | OpenAlex ID | C2779302956 |
| P10283 | OpenAlex ID | C2911059045 |
| P1550 | Orphanet ID | 1531 |
| P4233 | PatientsLikeMe condition ID | craniosyntosis |
| P3417 | Quora topic ID | Craniosynostosis |
| P4527 | UK Parliament thesaurus ID | 433669 |
| P2892 | UMLS CUI | C0010278 |
| P2892 | UMLS CUI | C0030044 |
| P2892 | UMLS CUI | C0235942 |
| P2892 | UMLS CUI | C0265535 |
| P2892 | UMLS CUI | C2750811 |
| P2892 | UMLS CUI | C4280665 |
| P2892 | UMLS CUI | C4280666 |
| P12086 | WikiKids ID | Craniosynostose |
| P11143 | WikiProjectMed ID | Craniosynostosis |
| P3471 | WikiSkripta article ID | 2178 |
| P2347 | YSO ID | 28456 |
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