Wikidata entity: Q16838027
| P2176 | drug or therapy used for treatment | ... | Q20801767 (pegademase bovine) | pegademase bovine |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2293 | genetic association | ... | Q14914108 (CIITA) | CIITA |
| P2293 | genetic association | ... | Q18031111 (RFX5) | RFX5 |
| P2293 | genetic association | ... | Q18031112 (RFXAP) | RFXAP |
| P2293 | genetic association | ... | Q18033164 (RFXANK) | RFXANK |
| P1995 | health specialty | ... | Q101929 (immunology) | immunology |
| P1995 | health specialty | ... | Q162606 (endocrinology) | endocrinology |
| P1995 | health specialty | ... | Q123028 (pediatrics) | pediatrics |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P1748 | NCI Thesaurus ID | String | C171268 | ??? |
| P1748 | NCI Thesaurus ID | String | C3895 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q1334408 (severe combined immunodeficiency) | severe combined immunodeficiency |
| P279 | subclass of | ... | Q3508735 (Bare lymphocyte syndrome) | Bare lymphocyte syndrome |
| P699 | Disease Ontology ID | DOID:5812 |
| P4317 | GARD rare disease ID | 824 |
| P7464 | Genetics Home Reference Conditions ID | bare-lymphocyte-syndrome-type-ii |
| P4229 | ICD-10-CM | D81.6 |
| P665 | KEGG ID | H00985 |
| P492 | OMIM ID | 209920 |
| P492 | OMIM ID | 209920 |
| P1550 | Orphanet ID | 572 |
| P2892 | UMLS CUI | C0242583 |
| P2892 | UMLS CUI | C2931418 |
| P11430 | UniProt disease ID | DI-00171 |
Why not click here or view trends?
log id: 2703333