Wikidata entity: Q18553536
| P373 | Commons category | String | Syndromes with intellectual disability | ??? |
| 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 | ... | Q18036648 (WDFY3) | WDFY3 |
| P2293 | genetic association | ... | Q18036678 (MYT1L) | MYT1L |
| P2293 | genetic association | ... | Q18036827 (KDM6B) | KDM6B |
| P2293 | genetic association | ... | Q18037142 (MED13L) | MED13L |
| P2293 | genetic association | ... | Q18037904 (AUTS2) | AUTS2 |
| P2293 | genetic association | ... | Q18041700 (ASXL2) | ASXL2 |
| P2293 | genetic association | ... | Q18043138 (TAOK1) | TAOK1 |
| P2293 | genetic association | ... | Q21163346 (CTCF) | CTCF |
| P2293 | genetic association | ... | Q4864556 (TRIO) | TRIO |
| P2293 | genetic association | ... | Q17835924 (KIF1A) | KIF1A |
| P2293 | genetic association | ... | Q18027119 (HOXA1) | HOXA1 |
| P2293 | genetic association | ... | Q18030282 (OPHN1) | OPHN1 |
| P2293 | genetic association | ... | Q18030728 (PPP2R5D) | PPP2R5D |
| P2293 | genetic association | ... | Q18031610 (SMS) | SMS |
| P2293 | genetic association | ... | Q18032252 (UBE2A) | UBE2A |
| P2293 | genetic association | ... | Q18032355 (NSD2) | NSD2 |
| P2293 | genetic association | ... | Q18032697 (KAT6A) | KAT6A |
| P2293 | genetic association | ... | Q18032981 (PPM1D) | PPM1D |
| P2293 | genetic association | ... | Q18033160 (CDK13) | CDK13 |
| P2293 | genetic association | ... | Q18033279 (CRADD) | CRADD |
| P2293 | genetic association | ... | Q18036517 (PUF60) | PUF60 |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| 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 | ... | Q183560 (intellectual disability) | intellectual disability |
| P910 | topic's main category | ... | Q30822641 (Category:Syndromes with intellectual disability) | Category:Syndromes with intellectual disability |
| P699 | Disease Ontology ID | DOID:0050888 |
| P5270 | Mondo ID | MONDO_0015162 |
| P1550 | Orphanet ID | 102369 |
| P2892 | UMLS CUI | C5681780 |
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