Wikidata entity: Q3338682
| 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 | ... | Q18032747 (GAN) | GAN |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P1692 | ICD-9-CM | String | 349.89 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C84728 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q10267817 (autosomal recessive disease) | autosomal recessive disease |
| P279 | subclass of | ... | Q18557549 (axonal neuropathy) | axonal neuropathy |
| P9272 | DeCS ID | 53516 |
| P699 | Disease Ontology ID | DOID:0090068 |
| P557 | DiseasesDB | 33515 |
| P4317 | GARD rare disease ID | 6500 |
| P7464 | Genetics Home Reference Conditions ID | giant-axonal-neuropathy |
| P3827 | JSTOR topic ID (archived) | giant-axonal-neuropathy |
| P665 | KEGG ID | H01259 |
| P486 | MeSH descriptor ID | D056768 |
| P672 | MeSH tree code | C10.500.300.490 |
| P672 | MeSH tree code | C10.574.500.495.490 |
| P672 | MeSH tree code | C10.668.829.325 |
| P672 | MeSH tree code | C10.668.829.800.300.490 |
| P672 | MeSH tree code | C16.131.666.300.490 |
| P672 | MeSH tree code | C16.320.400.375.490 |
| P6366 | Microsoft Academic ID (discontinued) | 2777893043 |
| P5270 | Mondo ID | MONDO_0000128 |
| P492 | OMIM ID | 256850 |
| P492 | OMIM ID | 256850 |
| P1550 | Orphanet ID | 643 |
| P3417 | Quora topic ID | Giant-Axonal-Neuropathy |
| P2892 | UMLS CUI | C1850386 |
| P2892 | UMLS CUI | C5200933 |
| P11143 | WikiProjectMed ID | Giant axonal neuropathy |
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