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
17,20-lyase deficiency, isolated 
17-alpha-hydroxylase/17,20-lyase deficiency, combined complete 
17-alpha-hydroxylase/17,20-lyase deficiency, combined partial 
Adamantinomatous Craniopharyngioma 
adrenal gland disease +   
autoimmune disorder of endocrine system +   
Bamforth-Lazarus syndrome 
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
campomelic dysplasia 
choledocholithiasis 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
duplication of the pituitary gland 
endocrine neoplasm +   
endocrine tuberculosis +  
familial hypocalciuric hypercalcemia +  
familial tumoral calcinosis +  
female athlete triad syndrome 
Follicular Variant Thyroid Gland Papillary Carcinoma 
Genetic bone tumor +  
Genetic cardiac tumor 
Genetic digestive tract tumor +  
Genetic endocrine tumor +   
An instance of neuroendocrine neoplasm that is caused by an inherited modification of the individual's genome.
Genetic eye tumor 
Genetic gynecological tumor +  
Genetic renal tumor +   
Genetic skin tumor +   
Genetic soft tissue tumor +   
Genetic tumor of hematopoietic and lymphoid tissues +   
Genetic urogenital tumor +  
genito-palato-cardiac syndrome 
gonadal disorder +   
hereditary endocrine growth disease +  
hyperinsulinemic hypoglycemia +  
hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 
hypoinsulinemic hypoglycemia and body hemihypertrophy 
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 
inherited obesity +  
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
liver disease +   
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
muscular pseudohypertrophy-hypothyroidism syndrome 
neuroendocrine disorder +  
NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction +  
Non-Neoplastic Bile Duct Disorder +   
Non-polyposis Turcot syndrome 
pancreas disease +   
Papillary Craniopharyngioma 
Papillary Tumor of the Pineal Region 
parathyroid disease +   
parneoplastic endocrine syndrome +  
pituitary deficiency +  
pituitary gland disease +   
polycystic ovary syndrome  
polyendocrinopathy +  
Poorly Differentiated Thyroid Gland Carcinoma +  
rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 
Rare genetic endocrine disease +   
thymus gland disorder +  
thymus hyperplasia 
thyroid disease +   
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
Wolfram-like syndrome 

Synonyms
Exact Synonyms: Orphanet:271847 ;   hereditary neuroendocrine neoplasm ;   http://linkedlifedata.com/resource/umls/id/CN202530 ;   inherited neuroendocrine tumor
Related Synonyms: genetic neuroendocrine tumor
Xrefs: ORDO:271847 ;   UMLS:CN202530
Definition Sources: MONDO:patterns/hereditary

paths to the root