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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

Property Value
dbo:description
  • Krankheit (de)
  • хвороба (uk)
  • avtosomno dominantna bolezen, ki ima materialno podlago v mutaciji gena za tumorski supresor MEN1; značilna je čezmerna aktivnost endokrinih žlez, ki pogosto vključuje tumorje obščitnic, hipofize in trebušne slinavke (sl)
  • aandoening van het endocrien systeem (nl)
  • 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)
dbo:diseasesDB
  • 7971
dbo:eMedicineSubject
  • med (en)
dbo:eMedicineTopic
  • 2404 (en)
dbo:icd10
  • D44.8
dbo:icd9
  • 258.01
dbo:icdo
  • 8360/1
dbo:medlinePlus
  • 000398
dbo:meshId
  • D018761
dbo:omim
  • 131100 (xsd:integer)
dbo:orpha
  • 652
dbo:thumbnail
dbo:wikiPageExternalLink
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dbp:caption
  • Multiple endocrine neoplasia type 1 is inherited in an autosomal dominant manner. (en)
dbp:diseasesdb
  • 7971 (xsd:integer)
dbp:emedicinesubj
  • med (en)
dbp:emedicinetopic
  • 2404 (xsd:integer)
dbp:icd
  • 258.010000 (xsd:double)
  • (en)
  • D44.8 (en)
dbp:icdo
  • 8360 (xsd:integer)
dbp:medlineplus
  • 398 (xsd:integer)
dbp:meshid
  • D018761 (en)
dbp:omim
  • 131100 (xsd:integer)
dbp:orphanet
  • 652 (xsd:integer)
dbp:synonyms
  • MEN-1 syndrome, Wermer's syndrome (en)
dbp:wikiPageUsesTemplate
dbp:wordnet_type
dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Multiple endocrine neoplasia type 1 (en)
  • تكون الورم الصماوي المتعدد النوع 1 (ar)
  • Neoplàsia endocrina múltiple tipus 1 (ca)
  • Néoplasie endocrinienne multiple type 1 (fr)
  • Neoplasia endócrina múltipla do tipo 1 (pt)
  • Синдром Вермера (ru)
  • Множинна ендокринна неоплазія тип 1 (uk)
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