multiple endocrine neoplasia type 1

Preferred Label : multiple endocrine neoplasia type 1;

MeSH definition : A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and the PANCREATIC ISLETS. The resulting clinical signs include HYPERPARATHYROIDISM; HYPERCALCEMIA; HYPERPROLACTINEMIA; CUSHING DISEASE; GASTRINOMA; and ZOLLINGER-ELLISON SYNDROME. This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene (GENES, TUMOR SUPPRESSOR) on CHROMOSOME 11 (Locus: 11q13).;

MeSH synonym : neoplasms, multiple endocrine type i; neoplasms, multiple endocrine type 1; multiple endocrine neoplasia type i; multiple endocrine neoplasms type 1; wermer syndrome; neoplasia, multiple endocrine type 1;

CISMeF synonym : men 1; men i; men1; mea 1; mea i;

MeSH annotation : coordinate IM with specific endocrine/neoplasm pre-coordinates (IM) specific histological type (IM) if pertinent;

Wikipedia link : https://en.wikipedia.org/wiki/Multiple endocrine neoplasia type 1;

Details

Origin ID

D018761;

UMLS CUI

C0025267;

Allowable qualifiers
- blood [MeSH Qualifier]
- blood supply [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- secondary [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- -1 (qualifier value) [SNOMED CT concept]
- 1 or more [EDAM data]
- 1+ Score [NCIt concept]
- 1+ Score, WHO [NCIt concept]
- Arabic numeral 1 (qualifier value) [Inactive SNOMED CT concept]
- Congenital myopathy 4b, autosomal recessive [OMIM Phenotype]
- Integer +1 (qualifier value) [SNOMED CT concept]
- MEN1 Gene [NCIt concept]
- MEN1 Gene Mutation [NCIt concept]
- MEN1 wt Allele [NCIt concept]
- Menin [NCIt concept]
- Menin 1 [OMIM gene]
- Multiple endocrine adenomatosis Type II [MedDRA LLT]
- Multiple endocrine neoplasia type II [PASCAL descriptor]
- Multiple endocrine neoplasia type III [PASCAL descriptor]
- One [NCIt concept]
- menin 1 [ORDO Gene]
Currated CISMeF NLP mapping
- MEA Type I [MedDRA LLT]
- MEN Type I [MedDRA LLT]
- Multiple Endocrine Neoplasia Type 1 [NCIt concept]
- Multiple endocrine adenomatosis Type I [MedDRA LLT]
- Multiple endocrine neoplasia Type 1 [MedDRA Preferred Term]
- Multiple endocrine neoplasia Type I [MedDRA LLT]
- Multiple endocrine neoplasia [MEN] type I [ICD-9 code]
- Multiple endocrine neoplasia type 1 [ICD-11 More detail]
- Multiple endocrine neoplasia type 1 [ORDO Disease]
- Multiple endocrine neoplasia type I [PASCAL descriptor]
- Multiple endocrine neoplasia, type 1 (disorder) [SNOMED CT concept]
- Multiple endocrine neoplasia, type I [OMIM Phenotype]
- multiple endocrine neoplasia type 1 [DO Concept]
- multiple endocrine neoplasia type 1 [Disease (Nov.)]
- multiple endocrine neoplasia, type 1 [SNOMED Notion]
DO Cross reference
- multiple endocrine neoplasia type 1 [DO Concept]
False automatic mappings
- Febrile seizures, familial, 1 [OMIM Phenotype]
Indexing information
- MEN1 protein, human [MeSH Supplementary Concept]
- Men1 protein, mouse [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- ACTH-dependent Cushing syndrome [ORDO Disease]
- ACTH-independent Cushing syndrome [ORDO Disease]
- Familial primary hyperparathyroidism [ORDO Disease]
- Genetic hyperparathyroidism [ORDO Disease]
- Inherited cancer-predisposing syndrome [ORDO Disease]
- Rare hyperparathyroidism [ORDO Disease]
- Rare parathyroid tumor [ORDO Disease]
ORDO relation(s)
- Multiple endocrine neoplasia type 1 [ORDO Disease]
Record concept(s)
- multiple endocrine neoplasia type 1 [MeSH concept]
See also
- gastrinoma [MeSH Descriptor]
- hyperparathyroidism [MeSH Descriptor]
- zollinger-ellison syndrome [MeSH Descriptor]
See also inter- (CISMeF)
- TPM3 wt Allele [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- MEA Type I [MedDRA LLT]
- MEN Type I [MedDRA LLT]
- Multiple Endocrine Neoplasia Type 1 [NCIt concept]
- Multiple endocrine adenomatosis Type I [MedDRA LLT]
- Multiple endocrine neoplasia Type 1 [MedDRA Preferred Term]
- Multiple endocrine neoplasia Type I [MedDRA LLT]
- Multiple endocrine neoplasia [MEN] type I [ICD-9 code]
- Multiple endocrine neoplasia type 1 [ORDO Disease]
- Multiple endocrine neoplasia, type 1 (disorder) [SNOMED CT concept]
- Multiple endocrine neoplasia, type I [OMIM Phenotype]
- multiple endocrine neoplasia type 1 [DO Concept]
- multiple endocrine neoplasia type 1 [Disease (Nov.)]
- multiple endocrine neoplasia, type 1 [SNOMED Notion]

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