MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, UMDF: 1= Disease, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, Myopathy, SANDO
Disease Browser
Parent Node:
expandEndocrine Gland Neoplasms (D004701)
Parent Node:
expandNeoplasms, Multiple Primary (D009378)
Parent Node:
expandNeoplastic Syndromes, Hereditary (D009386)
..Starting node
..expandMultiple Endocrine Neoplasia (D009377)

       Child Nodes:
........expandMultiple Endocrine Neoplasia Type 1 (D018761)
........expandMultiple Endocrine Neoplasia Type 2a (D018813) Child1
........expandMultiple Endocrine Neoplasia Type 2b (D018814) Child1
........expandMultiple Endocrine Neoplasia, Type IV (C567059)



 Sister Nodes: 
..expandAdenomatous Polyposis Coli (D011125) Child10
..expandBasal Cell Nevus Syndrome (D001478) Child1
..expandBirt-Hogg-Dube Syndrome (D058249)
..expandCancer, Familial, with In Vitro Radioresistance (C566179)
..expandCollagenoma, Familial Cutaneous (C562925)
..expandColorectal Neoplasms, Hereditary Nonpolyposis (D003123) Child10
..expandDiaphyseal medullary stenosis with malignant fibrous histiocytoma (C536169)
..expandDysplastic Nevus Syndrome (D004416)
..expandExostoses, Multiple Hereditary (D005097) Child14
..expandFamilial cylindromatosis (C536611)
..expandGenochondromatosis (C563215)
..expandHamartoma Syndrome, Multiple (D006223) Child10
..expandHemangioma, capillary infantile (C535860)
..expandHereditary Breast and Ovarian Cancer Syndrome (D061325)
..expandHereditary leiomyomatosis and renal cell cancer (C535516)
..expandJuvenile polyposis syndrome (C537702)
..expandLi-Fraumeni Syndrome (D016864) Child4
..expandMelanoma-Pancreatic Cancer Syndrome (C563985)
..expandMeningioma, familial (C537443)
..expandMultiple Endocrine Neoplasia (D009377) Child6
..expandMyelocytic leukemia-like syndrome, familial, chronic (C536093)
..expandNeurofibromatoses (D017253) Child13  LSDB C:1
..expandParagangliomas 2 (C566646)
..expandParagangliomas 3 (C565335)
..expandPeutz-Jeghers Syndrome (D010580)
..expandProstate Cancer, Hereditary, 12 (C567510)
..expandTuberous Sclerosis (D014402) Child4
..expandTurcot syndrome (C536928)
..expandWilms Tumor (D009396) Child10
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:8253
Name:Multiple Endocrine Neoplasia
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.
Alternative IDs:
ParentIDs:MESH:D004701|MESH:D009378|MESH:D009386
TreeNumbers:C04.588.322.400 |C04.651.600 |C04.700.630 |C16.320.700.630 |C19.344.400
Synonyms:Adenomatoses, Familial Endocrine |Adenomatoses, Multiple Endocrine |Adenomatosis, Familial Endocrine |Adenomatosis, Multiple Endocrine |Adenopathies, Multiple Endocrine |Adenopathy, Multiple Endocrine |Endocrine Adenomatoses, Familial |Endocrine Adenomatoses, M
Slim Mappings:Cancer|Endocrine system disease|Genetic disease (inborn)
Reference: MedGen: D009377
MeSH: D009377
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal