Wikidata entity: Q50349715
| 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 | ... | Q14914141 (SCN11A) | SCN11A |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C125388 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q3702898 (hereditary sensory and autonomic neuropathy) | hereditary sensory and autonomic neuropathy |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P279 | subclass of | ... | Q55785424 (autosomal dominant hereditary sensory and autonomic neuropathy) | autosomal dominant hereditary sensory and autonomic neuropathy |
| P699 | Disease Ontology ID | DOID:0070149 |
| P4317 | GARD rare disease ID | 12723 |
| P4317 | GARD rare disease ID | 12732 |
| P4229 | ICD-10-CM | G60.8 |
| P5270 | Mondo ID | MONDO_0014244 |
| P492 | OMIM ID | 615548 |
| P492 | OMIM ID | 615548 |
| P1550 | Orphanet ID | 391397 |
| P2892 | UMLS CUI | C3809882 |
| P11430 | UniProt disease ID | DI-03988 |
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log id: 2398424