Wikidata entity: Q7616509

Quantities
| P1193 | prevalence | 0.000128 |
| P1193 | prevalence | 0.000149 |
| P1193 | prevalence | 0.000217 |
| P1193 | prevalence | 0.000241 |
| P1193 | prevalence | 0.0002691 |
| P1193 | prevalence | 0.00026998 |
| P1193 | prevalence | 0.000457 |
| P373 | Commons category | String | Neurofibromatosis type 1 | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2293 | genetic association | ... | Q20782771 (NF1) | NF1 |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1199 | mode of inheritance | ... | Q116406 (autosomal dominant) | autosomal dominant |
| P1748 | NCI Thesaurus ID | String | C3273 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P5131 | possible medical findings | ... | Q602709 (Crowe sign) | Crowe sign |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q847605 (neurofibromatoses) | neurofibromatoses |
| P279 | subclass of | ... | Q17074582 (neuro-cardio-facial-cutaneous syndromes) | neuro-cardio-facial-cutaneous syndromes |
| P508 | BNCF Thesaurus ID | 51026 |
| P9272 | DeCS ID | 30295 |
| P1036 | Dewey Decimal Classification | 616.99383 |
| P699 | Disease Ontology ID | DOID:0111253 |
| P557 | DiseasesDB | 8937 |
| P673 | eMedicine ID | 1219222 |
| P673 | eMedicine ID | 342500 |
| P673 | eMedicine ID | 1112001 |
| P673 | eMedicine ID | 1177266 |
| P1417 | Encyclopædia Britannica Online ID | science/neurofibromatosis-type-1 |
| P646 | Freebase ID | /m/05qdqm |
| P4317 | GARD rare disease ID | 7866 |
| P668 | GeneReviews ID | NBK1109 |
| P668 | GeneReviews ID | NBK47312 |
| P494 | ICD-10 ID | Q85.0 |
| P7807 | ICD-11 ID (Foundation) | 337970533 |
| P7329 | ICD-11 ID (MMS) | LD2D.10 |
| P493 | ICD-9 ID | 237.71 |
| P665 | KEGG ID | H01437 |
| P3201 | Medical Dictionary for Regulatory Activities ID | 10029268 |
| P604 | MedlinePlus ID | 000847 |
| P604 | MedlinePlus ID | 000847 |
| P486 | MeSH descriptor ID | D009456 |
| P672 | MeSH tree code | C04.557.580.600.580.590.650 |
| P672 | MeSH tree code | C04.700.631.650 |
| P672 | MeSH tree code | C10.562.600.500 |
| P672 | MeSH tree code | C10.574.500.549.400 |
| P672 | MeSH tree code | C10.668.829.675 |
| P672 | MeSH tree code | C16.320.400.560.400 |
| P672 | MeSH tree code | C16.320.700.633.650 |
| P6366 | Microsoft Academic ID (discontinued) | 2778102573 |
| P6366 | Microsoft Academic ID (discontinued) | 2909696185 |
| P7995 | NHS Health A to Z ID | neurofibromatosis-type-1 |
| P492 | OMIM ID | 162210 |
| P492 | OMIM ID | 162210 |
| P492 | OMIM ID | 162200 |
| P492 | OMIM ID | 162200 |
| P10283 | OpenAlex ID | C2778102573 |
| P1550 | Orphanet ID | 636 |
| P3417 | Quora topic ID | Neurofibromatosis-Type-1 |
| P2892 | UMLS CUI | C0027831 |
| P11430 | UniProt disease ID | DI-02396 |
| P11143 | WikiProjectMed ID | Neurofibromatosis type I |
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