MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandneoplastic syndrome (MONDO:0021058)
..Starting node
..expandhereditary neoplastic syndrome ()

       Child Nodes:
........expandBAP1-related tumor predisposition syndrome ()
........expandblue rubber bleb nevus ()
........expandCarney-Stratakis syndrome ()
........expandcherubism ()
........expandchromosome 5q deletion syndrome ()
........expandCobb syndrome ()
........expandcombined immunodeficiency due to OX40 deficiency ()
........expandcommon variable immunodeficiency ()
........expandconstitutional mismatch repair deficiency syndrome ()
........expandDDX41-related hematologic malignancy predisposition syndrome ()
........expanddyskeratosis congenita ()
........expandfamilial atypical multiple mole melanoma syndrome ()
........expandfamilial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome ()
........expandfamilial isolated hyperparathyroidism ()
........expandfamilial multinodular goiter ()
........expandfamilial rhabdoid tumor ()
........expandhereditary breast ovarian cancer syndrome ()
........expandhereditary multiple osteochondromas ()
........expandhereditary retinoblastoma ()
........expandhereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome ()
........expandinherited digestive cancer-predisposing syndrome ()
........expandinherited renal cancer-predisposing syndrome ()
........expandKostmann syndrome ()
........expandLi-Fraumeni syndrome ()
........expandlymphoproliferative syndrome ()
........expandMaffucci syndrome ()
........expandmelanoma and neural system tumor syndrome ()
........expandMITF-related melanoma and renal cell carcinoma predisposition syndrome ()
........expandmultiple endocrine neoplasia ()
........expandmultiple self-healing squamous epithelioma ()
........expandN syndrome ()
........expandneurofibromatosis ()
........expandnevoid basal cell carcinoma syndrome ()
........expandOllier disease ()
........expandpigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome ()
........expandpolymalformative genetic syndrome with increased risk of developing cancer ()
........expandprogeroid features-hepatocellular carcinoma predisposition syndrome ()
........expandRothmund-Thomson syndrome ()
........expandSC phocomelia syndrome ()
........expandtuberous sclerosis ()



 Sister Nodes: 
..expandCarney triad ()
..expandectopic ACTH secretion syndrome ()
..expandectopic hormone secretion syndrome associated with neoplasia ()
..expandgrowing teratoma syndrome ()
..expandhereditary neoplastic syndrome ()
..expandMeigs syndrome ()
..expandmyelodysplastic syndrome ()
..expandPancoast syndrome ()
..expandRichter syndrome ()
..expandZollinger-Ellison syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15356
Name:hereditary neoplastic syndrome
Definition:The inherited predisposition toward getting a tumor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:cancer syndrome, hereditary; cancer syndromes, hereditary; familial neoplastic syndrome; familial tumor syndrome; hereditary cancer syndrome; hereditary cancer syndromes; hereditary neoplastic syndrome; hereditary neoplastic syndromes; hereditary tumor syndrome; inherited cancer syndrome; inherited
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal