rdfs: label
ar
de
en
fr
pt
pt-br
sl
"Infantile Myofibromatose"@de
"Miofibromatose da infância"@pt
"Miofibromatose da infância"@pt-br
"infantile myofibromatosis"@en
"infantilna miofibromatoza"@sl
"myofibromatose infantile"@fr
"ورم ليفي عضلي وليدي"@ar
skos: altLabel
"Fibromatosis, Congenital Generalized"@en
"IMF1"@en
"MYOFIBROMATOSIS, INFANTILE, 1"@en
"MYOFIBROMATOSIS, INFANTILE, 1; IMF1"@en
"Myofibromatosis, Infantile, type 1"@en
"Myofibromatosis, Juvenile"@en
"myofibromatosis"@en
schema: description
ar
de
en
uk
"Krankheit"@de
"connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
schema: dateModified
"2026-10-23T23:49:25+00:00"^^xsd:dateTime
schema: version
2560159304
wikibase: identifiers
19
22
wikibase: sitelinks
3
wikibase: statements
53
p: P11143
wd: statement/Q6029048-74A8D7E9-C950-4336-8A82-EC472CE190DF
p: P14914
wd: statement/Q6029048-FB5A23EA-24FB-4299-ADDF-EBF42EF1EABC
p: P1550
wd: statement/Q6029048-5dc0f548-489c-75c2-88df-ef142b37e2e8
p: P1692
wd: statement/Q6029048-0084FAE3-EFBF-4B9A-900B-90D23A95BDE3
p: P1748
wd: statement/Q6029048-7773E1BA-14C4-4176-9F93-7E50A061FC12
p: P1995
wd: statement/Q6029048-C45C2A05-E2DA-4EA3-B700-0A4052F57541
p: P2293
wd: statement/Q6029048-2671B2D8-F282-47C9-AA4E-D1903480F39B
wd: statement/Q6029048-3B25BF10-5FD0-40C1-AC19-9ECEF3CF9771
p: P279
wd: statement/Q6029048-b0c5c80c-4300-1a1d-a282-b45d9f3175b0
p: P2841
wd: statement/Q6029048-0949C0E2-3D78-43E2-B0AA-0A5BDAA4761F
wd: statement/Q6029048-5629760D-5F53-4F4C-A6D9-D922ECD63EA9
wd: statement/Q6029048-765D5B48-DB3D-4D1C-8223-D3ECFEF6E2BD
p: P2888
wd: statement/Q6029048-C1181415-FE5E-40FA-A7A5-662FF52555D4
wd: statement/Q6029048-E0453677-1E7D-413D-8D08-7937B4C089D1
wd: statement/Q6029048-FF15CB6A-0B86-45F6-9BC0-AB22515CABED
p: P2892
wd: statement/Q6029048-263A1AC7-BABC-467A-A5EF-39B4FAD1CCA7
wd: statement/Q6029048-75C3E15F-463C-4860-89ED-5D521666B592
p: P31
wd: statement/Q6029048-808B11D1-3C8E-4AC1-A21D-A825E0166454
wd: statement/Q6029048-FD17D458-F047-4B8D-A208-83CE26677831
p: P3841
wd: statement/Q6029048-92896AD6-5B34-49EC-86EA-DDBF143939E4
p: P4233
wd: statement/Q6029048-b0c07f85-4a58-d713-885c-318fcbcbcf54
p: P4317
wd: statement/Q6029048-0314FFCE-ADA1-4CD4-B246-7C929061C084
wd: statement/Q6029048-4E094943-92CB-4F44-9790-0557E4C24AD6
p: P486
wd: statement/Q6029048-E00C759D-F866-4DD6-8354-21B880FB6E84
p: P492
wd: statement/Q6029048-8E5D3B1F-D96E-40B1-915C-51CBE8153B91
wd: statement/Q6029048-94A33E29-B7CB-4BB4-9A54-A7152551B23A
p: P5008
wd: statement/Q6029048-230C031B-C978-4D80-98A1-449A4BA52800
p: P5270
wd: statement/Q6029048-A1F3FDB6-5F8E-49DC-95E7-CDEC8D023A82
p: P563
wd: statement/Q6029048-B39439AC-DCA0-4EE2-8114-17191C2EE7A1
p: P6366
wd: statement/Q6029048-9DA5CC0A-1471-4B5D-869B-990E034F9769
wd: statement/Q6029048-D2EA72B2-A4FF-41AB-8BE3-F5C6EE5BCA06
p: P6532
wd: statement/Q6029048-015E2E60-A18D-4574-ABF7-88EE981EFEB0
wd: statement/Q6029048-02F10288-6957-454A-82EE-1983F994F0E9
wd: statement/Q6029048-2610FC46-96C4-471F-9F45-8EF3768FC319
wd: statement/Q6029048-2F9D7A1A-0203-4DE4-9C0C-2A2A44FC1BC0
wd: statement/Q6029048-3348E857-4BEC-4611-95AF-1A4986C66F93
wd: statement/Q6029048-55C12091-D23E-4727-91CE-99062E70E7A3
wd: statement/Q6029048-57AFBF5B-5C4E-4986-9669-73C1D48B8079
wd: statement/Q6029048-6BE2C717-8F1B-4477-AFE0-0F4CDF38DE34
wd: statement/Q6029048-923A654D-61D1-4ABC-9E26-B9565C7AA4DC
wd: statement/Q6029048-996C0915-636A-4C51-B3DF-E74B806740B9
wd: statement/Q6029048-A780AB43-3D23-4DD2-A991-E302F7143811
wd: statement/Q6029048-A9913610-1EDF-498A-A8E6-F43C9E7B6B30
wd: statement/Q6029048-AE32B9BA-DF48-42ED-B361-C83CC60BD9B7
wd: statement/Q6029048-B42B9588-7630-4857-A518-48397576D1FF
wd: statement/Q6029048-C42C2BD6-7D13-490F-8619-3081CEEF0A58
wd: statement/Q6029048-CC49345B-D9C2-47AD-BEFC-03D1F54B3382
wd: statement/Q6029048-E1393842-7660-406B-8C50-A39225915970
p: P665
wd: statement/Q6029048-DB4D7C16-8C9D-41E8-BD0A-0E2F801F8BFA
p: P672
wd: statement/Q6029048-B81DDFD8-66BD-4EC7-BF76-A5AA23319453
p: P699
wd: statement/Q6029048-7F290BC8-089C-45D7-8427-DEC09671CD83
p: P7329
wd: statement/Q6029048-753abeb3-f291-4749-b295-bbcb3e2d9b2f
p: P7807
wd: statement/Q6029048-82AD099B-8795-4B44-B169-24CE04EAAC64
p: direct-normalized/P486
<http://id.nlm.nih.gov/mesh/D018224>
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0009227>
p: direct-normalized/P6366
<https://makg.org/entity/2776311014>
<https://makg.org/entity/2908901599>
p: direct-normalized/P665
<http://www.kegg.jp/entry/H01910>
p: direct-normalized/P672
<http://id.nlm.nih.gov/mesh/C04.557.450.565.590.550>
p: direct-normalized/P699
<http://purl.obolibrary.org/obo/DOID_DOID:0080109>
wdt: P11143
"Infantile myofibromatosis"
wdt: P14914
"D02591"
wdt: P1550
"2591"
wdt: P1692
"756.9"
wdt: P1748
"C3742"
wdt: P1995
oncology
wdt: P2293
NOTCH3
PDGFRB
wdt: P279
connective tissue benign neoplasm
wdt: P2841
congenital onset
neonatal onset
infantile onset
wdt: P2888
<http://identifiers.org/doid/DOID:0080109>
<http://purl.obolibrary.org/obo/DOID_0080109>
<http://www.orpha.net/ORDO/Orphanet_2591>
wdt: P2892
"C0206648"
"C0432284"
wdt: P31
type of disease
rare disease
wdt: P3841
"HP:0020135"
wdt: P4233
"infantile-myofibromatosis"
wdt: P4317
"2998"
"6163"
wdt: P486
"D018224"
wdt: P492
"228550"
"615293"
wdt: P5008
WikiProject Medicine
wdt: P5270
"MONDO_0009227"
wdt: P563
"8824/1"
wdt: P6366
"2776311014"
"2908901599"
wdt: P6532
gingival fibromatosis
kidney disease
abnormality of the metaphysis
Irregular hyperpigmentation
Benign neoplasm of the central nervous system
hypercalcemia
bowel obstruction
osteolysis
pancreatic cancer
sarcoma
eye disease
intestinal disease
fibroma
chondrocalcinosis
ulcer
tracheoesophageal fistula
bone cyst
wdt: P665
"H01910"
wdt: P672
"C04.557.450.565.590.550"
wdt: P699
"DOID:0080109"
wdt: P7329
"XH5MH2"
wdt: P7807
"563152712"