Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailble
Variant Visualizer (Genomic Variants)
unavailable
Gene Annotator (Functional Annotation)
Gene Annotator (Annotation Distribution)
Variant Visualizer (Genomic Variants)
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants) unavailble
Variant Visualizer (Damaging Variants)
unavailable
InterViewer (Protein-Protein Interactions)
GViewer (Genome Viewer)
Variant Visualizer (Damaging Variants)
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Gene Annotator (Annotation Comparison)
OLGA (Gene List Generator)
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
MOET (Multi-Ontology Enrichement)
GOLF (Gene-Ortholog Location Finder)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
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)
Diseases
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
Phenotypes & Models
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
Community
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)
EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS
{{ watchLinkText }}
Term:
hereditary neoplastic syndrome
go back to main search page
Accession:
EFO:MONDO:0015356
browse the term
Definition:
The inherited predisposition toward getting a tumor.
Synonyms:
exact_synonym:
NCIT:C3266; Orphanet:140162; familial neoplastic syndrome; familial tumor syndrome; familial tumour syndrome; hereditary cancer syndrome; hereditary cancer syndromes; hereditary neoplastic syndromes; hereditary tumor syndrome; hereditary tumour syndrome; http://identifiers.org/medgen/14326; http://identifiers.org/mesh/D009386; http://identifiers.org/snomedct/699346009; http://linkedlifedata.com/resource/umls/id/C0027672; inherited cancer syndrome; inherited cancer-predisposing syndrome
alt_id:
MONDO:0015356
xref:
GARD:19921
; MEDGEN:14326;
MESH:D009386
;
NCI:C3266
;
ORDO:140162
; SCTID:699346009; UMLS:C0027672
external_ontology:
predisposes_towards
predisposes_towards EFO:0000616
show annotations for term's descendants Sort by:
symbol
object name
position
reference
evidence
↑ asc
↓ desc
Rat (0)
Mouse (0)
Human (52)
Chinchilla (0)
Bonobo (0)
Dog (0)
Squirrel (0)
Pig (0)
Green Monkey (0)
Naked Mole-rat (0)
All
0 Annotations Found
Select a less specific term using the term browser
Term paths to the root
one shortest
all shortest
one longest
all longest
one shortest and longest
all
Path 1
Term
Annotations
experimental factor
0
material property
0
disposition
0
disease
0
genetic disorder
0
hereditary neoplastic syndrome
0
ATM-related cancer predisposition
0
BAP1-related tumor predisposition syndrome
0
BRCA1-related cancer predisposition
+
0
BRCA2-related cancer predisposition
+
0
Beckwith-Wiedemann syndrome
+
0
Brooke-Spiegler syndrome
+
0
CDH1-related diffuse gastric and lobular breast cancer syndrome
0
CHEK2-related cancer predisposition
0
Carney-Stratakis syndrome
0
DDX41-related hematologic malignancy predisposition syndrome
0
Kaposi sarcoma, susceptibility to
0
Kostmann syndrome
0
Li-Fraumeni syndrome
0
Maffucci syndrome
0
N syndrome
0
PALB2-related cancer predisposition
0
Proteus-like syndrome
0
Rothmund-Thomson syndrome
+
0
WAGR syndrome
+
0
Wiskott-Aldrich syndrome
0
basal cell carcinoma, susceptibility to, 7
0
blue rubber bleb nevus
0
cherubism
0
colorectal cancer, susceptibility to, 1
0
colorectal cancer, susceptibility to, 10
0
colorectal cancer, susceptibility to, 12
0
colorectal cancer, susceptibility to, 3
0
common variable immunodeficiency
+
0
dyskeratosis congenita
+
0
erythroleukemia, familial, susceptibility to
0
familial atypical multiple mole melanoma syndrome
0
familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
0
familial isolated hyperparathyroidism
+
0
familial multiple fibrofolliculoma
0
familial rhabdoid tumor
+
0
follicular lymphoma, susceptibility to, 1
0
glioma susceptibility
+
0
goiter, multinodular 1, with or without Sertoli-Leydig cell tumors
0
hereditary breast ovarian cancer syndrome
0
hereditary leiomyomatosis and renal cell cancer
0
hereditary multiple osteochondromas
+
0
hereditary nonpolyposis colon cancer
+
0
hereditary retinoblastoma
0
hereditary thrombocytopenia and hematologic cancer predisposition syndrome
+
0
hyperparathyroidism 2 with jaw tumors
0
intestinal polyposis syndrome
+
0
leukemia, acute lymphoblastic, susceptibility to, 3
0
leukemia, acute myeloid, susceptibility to
0
mismatch repair cancer syndrome 1
0
mosaic variegated aneuploidy syndrome
+
0
multiple endocrine neoplasia
+
0
multiple self-healing squamous epithelioma
0
nasopharyngeal carcinoma, susceptibility to, 1
0
neuroblastoma, susceptibility to, 1
0
neuroblastoma, susceptibility to, 2
0
neuroblastoma, susceptibility to, 3
0
neurofibromatosis
+
0
nevoid basal cell carcinoma syndrome
0
progeroid features-hepatocellular carcinoma predisposition syndrome
0
susceptibility to familial cutaneous melanoma
+
0
susceptibility to uveal melanoma
0
tuberous sclerosis
0
tumor predisposition syndrome 2
0
Path 2
Term
Annotations
experimental factor
0
material property
0
disposition
0
disease
0
cancer or benign tumor
0
neoplastic disease or syndrome
0
neoplastic syndrome
0
hereditary neoplastic syndrome
0
ATM-related cancer predisposition
0
BAP1-related tumor predisposition syndrome
0
BRCA1-related cancer predisposition
+
0
BRCA2-related cancer predisposition
+
0
Beckwith-Wiedemann syndrome
+
0
Brooke-Spiegler syndrome
+
0
CDH1-related diffuse gastric and lobular breast cancer syndrome
0
CHEK2-related cancer predisposition
0
Carney-Stratakis syndrome
0
DDX41-related hematologic malignancy predisposition syndrome
0
Kaposi sarcoma, susceptibility to
0
Kostmann syndrome
0
Li-Fraumeni syndrome
0
Maffucci syndrome
0
N syndrome
0
PALB2-related cancer predisposition
0
Proteus-like syndrome
0
Rothmund-Thomson syndrome
+
0
WAGR syndrome
+
0
Wiskott-Aldrich syndrome
0
basal cell carcinoma, susceptibility to, 7
0
blue rubber bleb nevus
0
cherubism
0
colorectal cancer, susceptibility to, 1
0
colorectal cancer, susceptibility to, 10
0
colorectal cancer, susceptibility to, 12
0
colorectal cancer, susceptibility to, 3
0
common variable immunodeficiency
+
0
dyskeratosis congenita
+
0
erythroleukemia, familial, susceptibility to
0
familial atypical multiple mole melanoma syndrome
0
familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
0
familial isolated hyperparathyroidism
+
0
familial multiple fibrofolliculoma
0
familial rhabdoid tumor
+
0
follicular lymphoma, susceptibility to, 1
0
glioma susceptibility
+
0
goiter, multinodular 1, with or without Sertoli-Leydig cell tumors
0
hereditary breast ovarian cancer syndrome
0
hereditary leiomyomatosis and renal cell cancer
0
hereditary multiple osteochondromas
+
0
hereditary nonpolyposis colon cancer
+
0
hereditary retinoblastoma
0
hereditary thrombocytopenia and hematologic cancer predisposition syndrome
+
0
hyperparathyroidism 2 with jaw tumors
0
intestinal polyposis syndrome
+
0
leukemia, acute lymphoblastic, susceptibility to, 3
0
leukemia, acute myeloid, susceptibility to
0
mismatch repair cancer syndrome 1
0
mosaic variegated aneuploidy syndrome
+
0
multiple endocrine neoplasia
+
0
multiple self-healing squamous epithelioma
0
nasopharyngeal carcinoma, susceptibility to, 1
0
neuroblastoma, susceptibility to, 1
0
neuroblastoma, susceptibility to, 2
0
neuroblastoma, susceptibility to, 3
0
neurofibromatosis
+
0
nevoid basal cell carcinoma syndrome
0
progeroid features-hepatocellular carcinoma predisposition syndrome
0
susceptibility to familial cutaneous melanoma
+
0
susceptibility to uveal melanoma
0
tuberous sclerosis
0
tumor predisposition syndrome 2
0