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 +  
biliary tract disease +   
blepharophimosis - intellectual disability syndrome, SBBYS type 
brain-lung-thyroid syndrome 
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 +  
female athlete triad syndrome 
Follicular Variant Thyroid Gland Papillary Carcinoma 
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
gonadal disorder +   
Hepatobiliary Neoplasm +   
hepatotoxicity 
hereditary endocrine growth disease +  
hereditary hemochromatosis type 1  
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 +   
A disease involving the liver. Any disease or dysfunction of the liver and the intrahepatic bile ducts. Pathological processes of the LIVER.
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
muscular pseudohypertrophy-hypothyroidism syndrome 
neuroendocrine disorder +  
Non-Neoplastic Bile Duct Disorder +   
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 +   
Rare genetic hepatic 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: DOID:409 ;   Disease of liver ;   Disorder of liver ;   Hepatopathy ;   LD - Liver disease ;   LIVER DIS ;   Liver Diseases ;   Liver Disorder ;   Liver Dysfunction ;   Liver Dysfunctions
Xrefs: DOID:409 ;   HP:0001392 ;   ICD10:K75 ;   ICD10:K76 ;   ICD10CM:K70-K77 ;   ICD9:573.8 ;   ICD9:573.9 ;   MEDGEN:893061 ;   MESH:D008107 ;   MONDO:0005154
External Ontologys: disease_has_location EFO:UBERON:0002107
Definition Sources: https://orcid.org/0000-0002-6601-2165

paths to the root