SHMARQL

multiple endocrine neoplasia type 1

<http://www.wikidata.org/entity/Q3347154>

autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas
rdfs:label
"multiple endocrine neoplasia type 1"@en
skos:altLabel
"Endocrine Adenomatosis, Multiple"@en
"Endocrine adenomatosis multiple"@en
"MEA Type 1"@en
"MEA Type I"@en
"MEN Type 1"@en
"MEN type I"@en
"MEN1"@en
"MEN1 syndrome"@en
"MULTIPLE ENDOCRINE NEOPLASIA, TYPE I"@en
"MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1"@en
"Mea 1"@en
"Men 1"@en
"Men1 Somatic Mutations"@en
"Multiple Endocrine Adenomatosis"@en
"Multiple Endocrine Adenomatosis Type 1"@en
"Multiple Endocrine Adenomatosis Type I"@en
"Multiple Endocrine Adenomatosis, Type I"@en
"Multiple Endocrine Neoplasia Type 1"@en
"Multiple Endocrine Neoplasia Type I"@en
"Wermer syndrome"@en
"Wermer's syndrome"@en
"multiple endocrine neoplasia type 1 syndrome"@en
schema:description
"autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas"@en
schema:dateModified "2026-10-24T00:29:24+00:00"^^xsd:dateTime
schema:version 2560166248
wikibase:identifiers 25
27
wikibase:sitelinks 13
wikibase:statements 61
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p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D018761>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0007540>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C04.588.322.400.500>
<http://id.nlm.nih.gov/mesh/C04.651.600.500>
<http://id.nlm.nih.gov/mesh/C04.700.630.500>
<http://id.nlm.nih.gov/mesh/C16.320.700.630.500>
<http://id.nlm.nih.gov/mesh/C19.344.400.500>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:10017>
wdt:P11143 "Multiple endocrine neoplasia type 1"
wdt:P11430 "DI-01593"
wdt:P1193 0.00005^^xsd:decimal
wdt:P1417 "science/multiple-endocrine-neoplasia-type-1"
wdt:P14914 "D00652"
wdt:P1550 "652"
wdt:P1692 "237.4"
"258.01"
wdt:P1748 "C3225"
wdt:P1995 oncology
endocrine surgery
wdt:P2293 MEN1
CDKN2B
CDKN1B
wdt:P279 multiple endocrine neoplasia
autosomal dominant disease
adrenal/paraganglial tumor
familial primary hyperparathyroidism
disease with Cushing syndrome as a major feature
inherited digestive cancer-predisposing syndrome
wdt:P2841 any age
wdt:P2888 <http://identifiers.org/doid/DOID:10017>
<http://purl.obolibrary.org/obo/DOID_10017>
<http://www.orpha.net/ORDO/Orphanet_652>
wdt:P2892 "C0025267"
"C3149237"
wdt:P31 type of disease
rare disease
wdt:P4229 "D44.8"
"E31.21"
wdt:P4233 "multiple-endocrine-neoplasia-type-1"
wdt:P4317 "3829"
wdt:P486 "D018761"
wdt:P492 "131100"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0007540"
wdt:P557 "7971"
wdt:P563 "8360/1"
wdt:P604 "000398"
wdt:P646 "/m/07n_zv"
wdt:P6532 Intestinal carcinoid
Pituitary gonadotropic cell adenoma
Pituitary thyrotropic cell adenoma
Decreased vigilance
Decreased male libido
Pulmonary carcinoid tumour
peptic ulcer disease
galactorrhea
primary hyperparathyroidism
parathyroid hyperplasia
impaired daily living skills
wdt:P672 "C04.588.322.400.500"
"C04.651.600.500"
"C04.700.630.500"
"C16.320.700.630.500"
"C19.344.400.500"
wdt:P673 "126438"
wdt:P6802 <http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal%20dominant%20-%20en.svg>
wdt:P699 "DOID:10017"
wdt:P9272 "32134"
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