Preferred Name | Multiple Endocrine Neoplasia | |
Synonyms |
Familial polyendocrine adenomatosis Multiple Endocrine Neoplasia Syndromes Endocrine adenomatosis MEA Multip endocr adenomatos MULTIPLE ENDOCRINE NEOPL SYNDROMES MEA Multiple endocrine adenomas Adenomatosis, Multiple Endocrine Adenomatosis, Familial Endocrine Multiple endocrine adenomatosis syndrome MULTIPLE ENDOCRINE NEOPL MEN-Multiple endocrine neoplas Neoplasms, Multiple Endocrine MEA Multiple endocrine adenomatosis MEN Multiple endocrine neoplasia MEN syndrome Multiple endocrine tumasia Multiple Endocrine Adenopathy Multple endocrine adenomatosis MEA SYNDROME |
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Definitions |
A group of autosomal dominant diseases characterized by the combined occurrence of tumors involving two or more ENDOCRINE GLANDS that secrete PEPTIDE HORMONES or AMINES. These neoplasias are often benign but can be malignant. They are classified by the endocrine glands involved and the degree of aggressiveness. The two major forms are MEN1 and MEN2 with gene mutations on CHROMOSOME 11 and CHROMOSOME 10, respectively. (source : MSH) |
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ID |
http://doe-generated-ontology.com/OntoAD#C0027662 |
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altLabel |
Familial polyendocrine adenomatosis Multiple Endocrine Neoplasia Syndromes Endocrine adenomatosis MEA Multip endocr adenomatos MULTIPLE ENDOCRINE NEOPL SYNDROMES MEA Multiple endocrine adenomas Adenomatosis, Multiple Endocrine Adenomatosis, Familial Endocrine Multiple endocrine adenomatosis syndrome MULTIPLE ENDOCRINE NEOPL MEN-Multiple endocrine neoplas Neoplasms, Multiple Endocrine MEA Multiple endocrine adenomatosis MEN Multiple endocrine neoplasia MEN syndrome Multiple endocrine tumasia Multiple Endocrine Adenopathy Multple endocrine adenomatosis MEA SYNDROME |
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definition |
A group of autosomal dominant diseases characterized by the combined occurrence of tumors involving two or more ENDOCRINE GLANDS that secrete PEPTIDE HORMONES or AMINES. These neoplasias are often benign but can be malignant. They are classified by the endocrine glands involved and the degree of aggressiveness. The two major forms are MEN1 and MEN2 with gene mutations on CHROMOSOME 11 and CHROMOSOME 10, respectively. (source : MSH) |
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disease_has_normal_tissue_origin | ||
hiddenLabel |
MultipleEndocrineNeoplasia |
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prefixIRI |
OntoAD:C0027662 |
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prefLabel |
Multiple Endocrine Neoplasia |
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subClassOf |
http://doe-generated-ontology.com/OntoAD#C0686496 |