SHMARQL

multiple endocrine neoplasia type 2A

<http://www.wikidata.org/entity/Q604075>

autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis
rdfs:label
"multiple endocrine neoplasia type 2A"@en
skos:altLabel
"MEA Type 2a"@en
"MEA Type II"@en
"MEN 2A"@en
"MEN Type 2a"@en
"MEN Type II"@en
"MEN-2A syndrome"@en
"MEN2A"@en
"MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA"@en
"MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A"@en
"Multiple Endocrine Adenomatosis Type 2a"@en
"Multiple Endocrine Adenomatosis Type II"@en
"Multiple Endocrine Adenomatosis, Type II"@en
"Multiple Endocrine Neoplasia Type 2a"@en
"Multiple Endocrine Neoplasia Type II"@en
"Multiple Endocrine Neoplasia, Type II"@en
"Pheochromocytoma and Amyloid-Producing Medullary Thyroid Carcinoma"@en
"Pheochromocytoma and amyloid producing medullary thyroid carcinoma"@en
"Ptc Syndrome"@en
"Sipple s Игорьyndrome"@en
"Thyroid Carcinoma, Familial Medullary"@en
"multiple endocrine neoplasia II"@en
schema:description
"autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis"@en
schema:dateModified "2026-10-23T23:45:39+00:00"^^xsd:dateTime
schema:version 2560158100
wikibase:identifiers 26
28
wikibase:sitelinks 11
wikibase:statements 47
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<http://id.nlm.nih.gov/mesh/C04.651.600.505>
<http://id.nlm.nih.gov/mesh/C04.700.630.505>
<http://id.nlm.nih.gov/mesh/C16.320.700.630.505>
<http://id.nlm.nih.gov/mesh/C19.344.400.505>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050430>
wdt:P10283 "C2776512331"
wdt:P11143 "Multiple endocrine neoplasia type 2"
wdt:P11430 "DI-02008"
wdt:P1417 "topic/multiple-endocrine-neoplasia-type-2A"
wdt:P14914 "D247698"
wdt:P1550 "247698"
wdt:P1692 "258.02"
wdt:P1748 "C3226"
wdt:P1995 oncology
wdt:P2293 RET
wdt:P279 multiple endocrine neoplasia
autosomal dominant disease
inherited renal tumor
catecholamine-producing tumor
wdt:P2841 childhood onset
wdt:P2888 <http://identifiers.org/doid/DOID:0050430>
<http://purl.obolibrary.org/obo/DOID_0050430>
<http://www.orpha.net/ORDO/Orphanet_247698>
<http://www.orpha.net/ORDO/Orphanet_653>
wdt:P2892 "C0025268"
"C1833921"
wdt:P31 type of disease
rare disease
wdt:P4229 "D44.8"
"E31.22"
wdt:P4233 "men2a"
wdt:P4317 "4881"
wdt:P486 "D018813"
wdt:P492 "171400"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0008234"
wdt:P557 "7984"
wdt:P604 "000399"
wdt:P6366 "2776512331"
wdt:P646 "/m/07p021"
wdt:P6532 Young adult onset
adult onset
hypertensive crisis
thyroid nodule
wdt:P668 "NBK1257"
wdt:P672 "C04.588.322.400.505"
"C04.651.600.505"
"C04.700.630.505"
"C16.320.700.630.505"
"C19.344.400.505"
wdt:P673 "123447"
wdt:P699 "DOID:0050430"
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