Wikidata entity: Q830308
| P373 | Commons category | String | Macular degeneration | ??? |
| 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 | None | ??? |
| P2293 | genetic association | ... | Q508356 (COL8A1) | COL8A1 |
| P2293 | genetic association | ... | Q14911975 (CFH) | CFH |
| P2293 | genetic association | ... | Q14914344 (TNXB) | TNXB |
| P2293 | genetic association | ... | Q17708694 (ABCA4) | ABCA4 |
| P2293 | genetic association | ... | Q18030185 (NOTCH4) | NOTCH4 |
| P2293 | genetic association | ... | Q18030830 (HTRA1) | HTRA1 |
| P2293 | genetic association | ... | Q18030967 (NECTIN2) | NECTIN2 |
| P2293 | genetic association | ... | Q14874317 (C3) | C3 |
| P2293 | genetic association | ... | Q14878192 (CETP) | CETP |
| P2293 | genetic association | ... | Q14886904 (GLI3) | GLI3 |
| P2293 | genetic association | ... | Q14911572 (TGFBR1) | TGFBR1 |
| P2293 | genetic association | ... | Q18051377 (B3GLCT) | B3GLCT |
| P2293 | genetic association | ... | Q18251054 (CFB) | CFB |
| P2293 | genetic association | ... | Q20970075 (CFI) | CFI |
| P2293 | genetic association | ... | Q18031016 (RAD51B) | RAD51B |
| P2293 | genetic association | ... | Q18031325 (RREB1) | RREB1 |
| P2293 | genetic association | ... | Q18031514 (SKIV2L) | SKIV2L |
| P2293 | genetic association | ... | Q18035395 (TOMM40) | TOMM40 |
| P2293 | genetic association | ... | Q18035445 (FBLN5) | FBLN5 |
| P2293 | genetic association | ... | Q18047300 (HMCN1) | HMCN1 |
| P2293 | genetic association | ... | Q85942926 (monophenol monooxygenase) | monophenol monooxygenase |
| P1995 | health specialty | ... | Q161437 (ophthalmology) | ophthalmology |
| P1692 | ICD-9-CM | String | 362.50 | ??? |
| P667 | ICPC 2 ID | String | F84 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q3842207 (maculopathy) | maculopathy |
| P31 | instance of | ... | Q112965645 (symptom or sign) | symptom or sign |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C84391 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P989 | spoken text audio | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/Macular%20degeneration.ogg | ??? |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q737460 (visual impairment) | visual impairment |
| P279 | subclass of | ... | Q16678480 (degeneration of macula and posterior pole) | degeneration of macula and posterior pole |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P279 | subclass of | ... | Q27429789 (macular degeneration) | macular degeneration |
| P699 | Disease Ontology ID | DOID:10871 |
| P557 | DiseasesDB | 11948 |
| P673 | eMedicine ID | 1223154 |
| P10565 | Encyclopedia of China (Third Edition) ID | 235477 |
| P1417 | Encyclopædia Britannica Online ID | topic/age-related-macular-degeneration |
| P11956 | Experimental Factor Ontology ID | 0001365 |
| P646 | Freebase ID | /m/03mmxd |
| P7464 | Genetics Home Reference Conditions ID | age-related-macular-degeneration |
| P3841 | Human Phenotype Ontology ID | HP:0007868 |
| P4229 | ICD-10-CM | H35.30 |
| P7807 | ICD-11 ID (Foundation) | 1514301548 |
| P7329 | ICD-11 ID (MMS) | 9B75.0 |
| P3827 | JSTOR topic ID (archived) | macular-degeneration |
| P8408 | KBpedia ID | MacularDegeneration |
| P665 | KEGG ID | H00821 |
| P604 | MedlinePlus ID | 001000 |
| P604 | MedlinePlus ID | 001000 |
| P7995 | NHS Health A to Z ID | age-related-macular-degeneration-amd |
| P1461 | Patientplus ID | age-related-macular-degeneration-pro |
| P5806 | SNOMED CT ID | 267718000 |
| P2892 | UMLS CUI | C0242383 |
| P12800 | Vikidia article ID | fr:Dégénérescence_maculaire_liée_à_l'âge |
| P3471 | WikiSkripta article ID | 80455 |
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