Wikidata entity: Q474254
| 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) | ??? |
| P2293 | genetic association | ... | Q14878377 (PTEN) | PTEN |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1995 | health specialty | ... | Q162555 (oncology) | oncology |
| P1692 | ICD-9-CM | String | 759.6 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C3939 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q18554834 (penile disease) | penile disease |
| P279 | subclass of | ... | Q55785288 (multiple congenital anomalies/dysmorphic syndrome-intellectual disability) | multiple congenital anomalies/dysmorphic syndrome-intellectual disability |
| P279 | subclass of | ... | Q55785835 (genetic skin vascular disorder) | genetic skin vascular disorder |
| P279 | subclass of | ... | Q55785866 (genetic syndromic intellectual disability) | genetic syndromic intellectual disability |
| P279 | subclass of | ... | Q55786077 (complex vascular malformation with associated anomalies) | complex vascular malformation with associated anomalies |
| P279 | subclass of | ... | Q55786847 (inherited digestive tract tumor) | inherited digestive tract tumor |
| P279 | subclass of | ... | Q55788290 (rare genetic vascular tumor) | rare genetic vascular tumor |
| P279 | subclass of | ... | Q55789072 (rare nervous system tumor) | rare nervous system tumor |
| P279 | subclass of | ... | Q179630 (syndrome) | syndrome |
| P279 | subclass of | ... | Q3508737 (multiple hamartoma syndrome) | multiple hamartoma syndrome |
| P279 | subclass of | ... | Q7113674 (overgrowth syndrome) | overgrowth syndrome |
| P279 | subclass of | ... | Q9303627 (brain cancer) | brain cancer |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P699 | Disease Ontology ID | DOID:0050657 |
| P557 | DiseasesDB | 31337 |
| P646 | Freebase ID | /m/0bdch8 |
| P4317 | GARD rare disease ID | 5887 |
| P668 | GeneReviews ID | NBK1488 |
| P4229 | ICD-10-CM | Q87.8 |
| P4229 | ICD-10-CM | Q87.89 |
| P7807 | ICD-11 ID (Foundation) | 357383447 |
| P6366 | Microsoft Academic ID (discontinued) | 2778630296 |
| P5270 | Mondo ID | MONDO_0007924 |
| P492 | OMIM ID | 158350 |
| P492 | OMIM ID | 158350 |
| P1550 | Orphanet ID | 109 |
| P4233 | PatientsLikeMe condition ID | brrs |
| P2892 | UMLS CUI | C0265326 |
| P11143 | WikiProjectMed ID | Bannayan–Riley–Ruvalcaba syndrome |
| P3471 | WikiSkripta article ID | 52944 |
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