Wikidata entity: Q1332427
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 758.6 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C61420 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q130487634 (intersex variation) | intersex variation |
| P279 | subclass of | ... | Q938107 (hypogonadism) | hypogonadism |
| P279 | subclass of | ... | Q18554938 (sex differentiation disease) | sex differentiation disease |
| P2581 | BabelNet ID | 03376824n |
| P2581 | BabelNet ID | 03376824n |
| P699 | Disease Ontology ID | DOID:14447 |
| P646 | Freebase ID | /m/02p9mm9 |
| P4317 | GARD rare disease ID | 2538 |
| P6417 | Homosaurus ID (V2) | gonadalDysgenesis |
| P10192 | Homosaurus ID (V3) | homoit0000599 |
| P13438 | Homosaurus ID (V4) | homoit0000599 |
| P494 | ICD-10 ID | Q99.1 |
| P3827 | JSTOR topic ID (archived) | gonadal-dysgenesis |
| P3201 | Medical Dictionary for Regulatory Activities ID | 10019906 |
| P486 | MeSH descriptor ID | D006059 |
| P672 | MeSH tree code | C12.050.351.875.253.309 |
| P672 | MeSH tree code | C12.200.706.316.309 |
| P672 | MeSH tree code | C12.800.316.309 |
| P672 | MeSH tree code | C16.131.939.316.309 |
| P672 | MeSH tree code | C19.391.119.309 |
| P6366 | Microsoft Academic ID (discontinued) | 2778324535 |
| P6366 | Microsoft Academic ID (discontinued) | 2910449836 |
| P11250 | Miraheze article ID | lgbta:Gonadal_Dysgenesis |
| P5270 | Mondo ID | MONDO_0001967 |
| P691 | NL CR AUT ID | ph122516 |
| P10283 | OpenAlex ID | C2778324535 |
| P2892 | UMLS CUI | C0018051 |
Why not click here or view trends?
log id: 9539743