neurofibromatosis type 6

medical condition
rdfs:label
"neurofibromatosis type 6"@en
skos:altLabel "Autosomal dominant café au lait spots"@en
"CAFE-AU-LAIT SPOTS, MULTIPLE"@en
"Familial cafC)-au-lait spots"@en
"Familial cafeB4-au-lait spots"@en
"Familial cafe´-au-lait spots"@en
"Familial café-au-lait spots"@en
"Familial multiple cafe-au-lait spots"@en
"Multiple cafC)-au-lait spots"@en
"Multiple cafC)-au-lait syndrome"@en
"Multiple cafeB4-au-lait spots"@en
"Multiple cafeB4-au-lait syndrome"@en
"Multiple cafe´-au-lait spots"@en
"Multiple cafe´-au-lait syndrome"@en
"Multiple café-au-lait spots"@en
"Multiple café-au-lait syndrome"@en
"NF6"@en
"Neurofibromatosis type 6"@en
schema:description
"medical condition"@en
schema:dateModified "2026-10-23T23:52:34+00:00"^^xsd:dateTime
schema:version 2560159864
wikibase:identifiers 9
wikibase:sitelinks 1
wikibase:statements 17
p:P14914 wd:statement/Q55780397-6482FB78-55E1-49A6-B336-605B257AF31C
p:P1550 wd:statement/Q55780397-351726FF-7DE4-4C8C-825D-A6F722BE04A3
p:P2293 wd:statement/Q55780397-DB6A17AE-05AA-42A0-AEC3-970DA532E56F
p:P279 wd:statement/Q55780397-FBF51263-5F0D-43E5-9711-CAF430EB2917
p:P2841 wd:statement/Q55780397-63433258-8DDD-429A-AEE2-782A687DD189
p:P2888 wd:statement/Q55780397-AF3DB42B-0107-485D-9B23-EB9BF66C9188
wd:statement/Q55780397-BA9F470B-AF03-4225-81B8-249095140D7D
p:P2892 wd:statement/Q55780397-3B8110F2-5A81-4CB8-876E-0CF7D63A68EE
p:P31 wd:statement/Q55780397-2FC6FE36-4727-417E-ACCF-7F08668D3666
p:P3841 wd:statement/Q55780397-B61B4D08-326B-468F-977C-0453E46FDE3B
p:P4229 wd:statement/Q55780397-1A896956-AF07-4B4A-A46F-F20DABE3070E
p:P4317 wd:statement/Q55780397-13F56354-3B57-45A0-AAB8-2403B653836E
p:P486 wd:statement/Q55780397-7E976CF6-4A89-4438-846C-34C1DAA29A61
p:P492 wd:statement/Q55780397-D4BDD2DB-CB46-4A8A-9E37-14E006277D43
p:P5270 wd:statement/Q55780397-ED9A7F3C-7290-4DC0-9329-25E7F6DFC194
p:P6532 wd:statement/Q55780397-D1CAA443-8B05-4314-AEB1-22B5526CBD1C
wd:statement/Q55780397-FA99AB6B-E60F-43D8-9413-F3EE6C94EDF2
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C537421>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0007245>
wdt:P14914 "D02678"
wdt:P1550 "2678"
wdt:P2293 LZTR1
wdt:P279 hyperpigmentation of the skin
wdt:P2841 childhood onset
wdt:P2888 <http://purl.obolibrary.org/obo/HP_0007565>
<http://www.orpha.net/ORDO/Orphanet_2678>
wdt:P2892 "C1861975"
wdt:P31 type of disease
wdt:P3841 "HP:0007565"
wdt:P4229 "L81.3"
wdt:P4317 "3967"
wdt:P486 "C537421"
wdt:P492 "114030"
wdt:P5270 "MONDO_0007245"
wdt:P6532 neurofibromatosis type 6
melanosis
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