Wikidata entity: Q749409

| P373 | Commons category | String | Osteogenesis imperfecta | ??? |
| 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 | Ontology Lookup Service (OLS) | ??? |
| P1325 | external data available at URL | Url | None | ??? |
| P2293 | genetic association | ... | Q14881725 (COL1A1) | COL1A1 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 756.51 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q42303753 (designated intractable/rare disease) | designated intractable/rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C99003 | ??? |
| P1748 | NCI Thesaurus ID | String | C26837 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q3251367 (osteochondrodysplasia) | osteochondrodysplasia |
| P1617 | BBC Things ID | 50072515-5e41-45ab-bd09-2300b8b0aafd |
| P508 | BNCF Thesaurus ID | 21888 |
| P8072 | CAB ID | 68362 |
| P9272 | DeCS ID | 10192 |
| P1036 | Dewey Decimal Classification | 571.948 |
| P699 | Disease Ontology ID | DOID:12347 |
| P557 | DiseasesDB | 866596 |
| P1417 | Encyclopædia Britannica Online ID | science/osteogenesis-imperfecta |
| P646 | Freebase ID | /m/03m7vl |
| P4317 | GARD rare disease ID | 1017 |
| P7464 | Genetics Home Reference Conditions ID | osteogenesis-imperfecta |
| P494 | ICD-10 ID | Q78.078.0 |
| P4229 | ICD-10-CM | Q78.0 |
| P7807 | ICD-11 ID (Foundation) | 1219932551 |
| P7329 | ICD-11 ID (MMS) | LD24.K0 |
| P493 | ICD-9 ID | 756.51756.51 |
| P3827 | JSTOR topic ID (archived) | osteogenesis-imperfecta |
| P665 | KEGG ID | H00506 |
| P604 | MedlinePlus ID | 001573 |
| P604 | MedlinePlus ID | 001573 |
| P486 | MeSH descriptor ID | D010013 |
| P672 | MeSH tree code | C05.116.099.708.685 |
| P672 | MeSH tree code | C16.320.737 |
| P672 | MeSH tree code | C17.300.200.540 |
| P6366 | Microsoft Academic ID (discontinued) | 2777668750 |
| P6366 | Microsoft Academic ID (discontinued) | 2909499170 |
| P6366 | Microsoft Academic ID (discontinued) | 2909773098 |
| P8189 | National Library of Israel J9U ID | 987007553341805171 |
| P950 | National Library of Spain SpMaBN ID (BNE v1.0) | XX553344 |
| P3222 | NE.se ID | osteogenesis-imperfecta |
| P691 | NL CR AUT ID | ph943941 |
| P492 | OMIM ID | 166200 |
| P492 | OMIM ID | 166200 |
| P10283 | OpenAlex ID | C2777668750 |
| P1550 | Orphanet ID | 666 |
| P1461 | Patientplus ID | osteogenesis-imperfecta |
| P4233 | PatientsLikeMe condition ID | osteogenesis-imperfecta |
| P3417 | Quora topic ID | Osteogenesis-Imperfecta |
| P2892 | UMLS CUI | C0023931 |
| P2892 | UMLS CUI | C0029434 |
| P12800 | Vikidia article ID | fr:Maladie_des_os_de_verre |
| P12086 | WikiKids ID | Osteogenesis_imperfecta |
| P11143 | WikiProjectMed ID | Osteogenesis imperfecta |
| P3471 | WikiSkripta article ID | 3829 |
| P4839 | Wolfram Language entity code | Entity["Disease", {"ICDNine756.51", "Primary"}] |
| P2347 | YSO ID | 20558 |
| P3553 | Zhihu topic ID | 19828949 |
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