Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
ATM-related cancer predisposition 
Axenfeld-Rieger syndrome +  
BAP1-related tumor predisposition syndrome 
basal cell carcinoma, susceptibility to, 7 
Beckwith-Wiedemann syndrome +  
blue rubber bleb nevus 
BRCA1-related cancer predisposition +  
BRCA2-related cancer predisposition +  
Brooke-Spiegler syndrome +  
Carney triad 
Carney-Stratakis syndrome 
CDH1-related diffuse gastric and lobular breast cancer syndrome 
central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease 
central hypoventilation syndrome, late-onset 
CHARGE syndrome 
CHEK2-related cancer predisposition 
cherubism 
colorectal cancer, susceptibility to, 1 
colorectal cancer, susceptibility to, 10 
colorectal cancer, susceptibility to, 12 
colorectal cancer, susceptibility to, 3 
common variable immunodeficiency +   
craniofacial microsomia  
craniofrontonasal syndrome 
DDX41-related hematologic malignancy predisposition syndrome 
dyskeratosis congenita +  
erythroleukemia, familial, susceptibility to 
familial atypical multiple mole melanoma syndrome 
familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome 
familial isolated hyperparathyroidism +  
familial multiple fibrofolliculoma 
familial rhabdoid tumor +  
follicular lymphoma, susceptibility to, 1 
glioma susceptibility +  
goiter, multinodular 1, with or without Sertoli-Leydig cell tumors 
hereditary breast ovarian cancer syndrome 
hereditary leiomyomatosis and renal cell cancer 
hereditary multiple osteochondromas +  
hereditary nonpolyposis colon cancer +  
hereditary retinoblastoma 
hereditary thrombocytopenia and hematologic cancer predisposition syndrome +  
Hirschsprung disease  
hyperparathyroidism 2 with jaw tumors 
intestinal polyposis syndrome +  
Kaposi sarcoma, susceptibility to 
Kostmann syndrome 
leukemia, acute lymphoblastic, susceptibility to, 3 
leukemia, acute myeloid, susceptibility to 
Li-Fraumeni syndrome 
Maffucci syndrome 
melanocytic neoplasm +   
mismatch repair cancer syndrome 1 
mosaic variegated aneuploidy syndrome +  
multiple endocrine neoplasia +  
Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs.
multiple self-healing squamous epithelioma 
N syndrome 
nasopharyngeal carcinoma, susceptibility to, 1 
neuroblastoma +   
neuroblastoma, susceptibility to, 1 
neuroblastoma, susceptibility to, 2 
neuroblastoma, susceptibility to, 3 
neurofibromatosis +  
neurofibromatosis type 1 +  
nevoid basal cell carcinoma syndrome 
PALB2-related cancer predisposition 
Paraganglioma +  
piebaldism 
progeroid features-hepatocellular carcinoma predisposition syndrome 
Proteus-like syndrome 
Riley-Day syndrome 
Rothmund-Thomson syndrome +  
susceptibility to familial cutaneous melanoma +  
susceptibility to uveal melanoma 
tuberous sclerosis 
tumor predisposition syndrome 2 
Waardenburg-Shah syndrome +  
WAGR syndrome +  
Wiskott-Aldrich syndrome 

Synonyms
Exact Synonyms: DOID:3125 ;   NCIT:C6432 ;   Orphanet:276161 ;   http://identifiers.org/medgen/45036 ;   http://identifiers.org/mesh/D009377 ;   http://identifiers.org/snomedct/46724008 ;   http://linkedlifedata.com/resource/umls/id/C0027662 ;   https://omim.org/phenotypicSeries/PS131100 ;   men ;   men syndrome
Synonyms: http://identifiers.org/meddra/10061299
Alternate IDs: MONDO:0017169
Xrefs: DOID:3125 ;   GARD:21044 ;   ICD9:258.0 ;   ICDO:8360/1 ;   MEDGEN:45036 ;   MESH:D009377 ;   MIM:PS131100 ;   MedDRA:10061299 ;   NANDO:2100148 ;   NCI:C6432
Definition Sources: Orphanet:276161

paths to the root