Wikidata entity: Q27429766
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2293 | genetic association | ... | Q24292611 (SGCD) | SGCD |
| P2293 | genetic association | ... | Q14885337 (DYSF) | DYSF |
| P2293 | genetic association | ... | Q18031464 (SGCA) | SGCA |
| P2293 | genetic association | ... | Q18031465 (SGCB) | SGCB |
| P2293 | genetic association | ... | Q18031467 (SGCG) | SGCG |
| P2293 | genetic association | ... | Q18036619 (TRIM32) | TRIM32 |
| P2293 | genetic association | ... | Q18053300 (ANO5) | ANO5 |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q1531322 (limb-girdle muscular dystrophy) | limb-girdle muscular dystrophy |
| P279 | subclass of | ... | Q10267817 (autosomal recessive disease) | autosomal recessive disease |
| P699 | Disease Ontology ID | DOID:0110274 |
| P4229 | ICD-10-CM | G71.0 |
| P7807 | ICD-11 ID (Foundation) | 319162980 |
| P7329 | ICD-11 ID (MMS) | 8C70.41 |
| P486 | MeSH descriptor ID | C538640 |
| P5270 | Mondo ID | MONDO_0015152 |
| P1550 | Orphanet ID | 102015 |
| P2892 | UMLS CUI | C2931907 |
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log id: 5684965