Wikidata entity: Q3043135
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2293 | genetic association | ... | Q18028496 (LCT) | LCT |
| P1542 | has effect | ... | Q219223 (lactose intolerance) | lactose intolerance |
| P1692 | ICD-9-CM | String | 271.3 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P361 | part of | ... | Q2567857 (Finnish heritage disease) | Finnish heritage disease |
| P279 | subclass of | ... | Q5662069 (lactase deficiency) | lactase deficiency |
| P279 | subclass of | ... | Q6013981 (carbohydrate metabolic disorder) | carbohydrate metabolic disorder |
| P279 | subclass of | ... | Q10267817 (autosomal recessive disease) | autosomal recessive disease |
| P279 | subclass of | ... | Q55785308 (congenital intestinal disease due to an enzymatic defect) | congenital intestinal disease due to an enzymatic defect |
| P279 | subclass of | ... | Q55785312 (metabolic disease with intestinal involvement) | metabolic disease with intestinal involvement |
| P279 | subclass of | ... | Q55787291 (disorder of carbohydrate absorption and transport) | disorder of carbohydrate absorption and transport |
| P699 | Disease Ontology ID | DOID:0111646 |
| P4317 | GARD rare disease ID | 12311 |
| P494 | ICD-10 ID | E73.0 |
| P4229 | ICD-10-CM | E73.0 |
| P7807 | ICD-11 ID (Foundation) | 2109252471 |
| P7329 | ICD-11 ID (MMS) | 5C61.61 |
| P665 | KEGG ID | H00116 |
| P3201 | Medical Dictionary for Regulatory Activities ID | 10086148 |
| P486 | MeSH descriptor ID | C562600 |
| P5270 | Mondo ID | MONDO_0009115 |
| P492 | OMIM ID | 223000 |
| P492 | OMIM ID | 223000 |
| P1550 | Orphanet ID | 53690 |
| P2892 | UMLS CUI | C0268179 |
| P11430 | UniProt disease ID | DI-01406 |
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