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 Behavioral & Substance Use Disorder 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 +   
autoimmune disorder of gastrointestinal tract +   
Bamforth-Lazarus syndrome 
benign digestive system neoplasm +   
beta thalassemia +  
blepharophimosis - intellectual disability syndrome, SBBYS type 
campomelic dysplasia 
caudal duplication 
chemotherapy-induced gastrointestinal mucositis 
Chilaiditi Syndrome 
choledocholithiasis 
colon diverticulum 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
common mesentery 
congenital enteropathy due to enteropeptidase deficiency 
Cronkhite-Canada syndrome 
Cushing syndrome +   
diarrheal disease +   
digestive duplication 
Digestive System Adenoma +   
digestive system cancer +   
digestive system infectious disorder +   
digestive system neuroendocrine neoplasm +   
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
disease of peritoneum +   
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
diverticulosis of bowel, hernia, and retinal detachment 
duplication of the pituitary gland 
dysplastic oral keratinocyte 
endocrine neoplasm +   
endocrine tuberculosis +  
enterocolitis +   
epiglottitis +  
esophageal disease +   
familial hypocalciuric hypercalcemia +  
female athlete triad syndrome 
flatulence  
Follicular Variant Thyroid Gland Papillary Carcinoma 
gastric outlet obstruction 
gastroesophageal disease 
gastrointestinal disease +   
gastrointestinal polyp +   
gastrointestinal ulceration, recurrent, with dysfunctional platelets 
Genetic digestive tract tumor +  
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
gonadal disorder +   
growth retardation-mild developmental delay-chronic hepatitis syndrome 
hepatobiliary disease +   
hereditary endocrine growth disease +  
hereditary mixed polyposis syndrome 
hyperinsulinemic hypoglycemia +  
hyperplastic polyposis syndrome +  
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 +  
intestinal disease +   
juvenile polyposis syndrome +  
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
lingual thyroid 
liver disease +   
Meckel's diverticulum 
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
mouth disease +   
Moyamoya disease with early-onset achalasia 
muscular pseudohypertrophy-hypothyroidism syndrome 
nasopharyngitis +  
neoplasm of oropharynx +   
neuroendocrine disorder +  
NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction +  
Non-Neoplastic Bile Duct Disorder +   
pancreas disease +   
A non-neoplastic or neoplastic disorder that affects the pancreas. Representative examples of non-neoplastic disorders include pancreatitis and pancreatic insufficiency. Representative examples of neoplastic disorders include cystadenomas, carcinomas, lymphomas, and neuroendocrine neoplasms. A non-neoplastic or neoplastic disorder that affects the pancreas. Representative examples of non-neoplastic disorders include pancreatitis and pancreatic insufficiency. Representative examples of neoplastic disorders include cystadenomas, carcinomas, lymphomas, and neuroendocrine neoplasms. [ NCIt:C26842 ]
Papillary Craniopharyngioma 
Papillary Tumor of the Pineal Region 
parathyroid disease +   
parneoplastic endocrine syndrome +  
peptic ulcer disease +   
periodontitis +   
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 +   
small intestine enteropathy  
splenic infarction 
stomach disease +   
stomach diverticulum 
thoraco-abdominal enteric duplication 
thymus gland disorder +  
thymus hyperplasia 
thyroid disease +   
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
tonsillitis +   
umbilical cord ulceration-intestinal atresia syndrome 
Wolfram-like syndrome 

Synonyms
Exact Synonyms: disease of pancreas;  disease or disorder of pancreas;  disorder of pancreas;  pancreas disease or disorder;  pancreas disorder;  pancreas problem;  pancreatic disorder
Related Synonyms: diseases, pancreatic;  pancreatic disease
Xrefs: DOID:26;  ICD10:E16;  ICD10:K86;  ICD9:577.8;  ICD9:577.9;  MEDGEN:14583;  MESH:D010182;  MONDO:0002356;  MedDRA:10033616;  NCI:C26842 ... show 2 more
External Ontologys: disease_has_location EFO:UBERON:0001264
Definition Sources: NCIT:C26842

paths to the root