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
abdominal wall malformation +  
angioosteohypertrophic syndrome 
ankyloblepharon filiforme-imperforate anus syndrome 
anotia 
Becker nevus syndrome +  
blindness - scoliosis - arachnodactyly syndrome 
bone fragility with contractures, arterial rupture, and deafness 
central nervous system malformation +  
cleft palate +  
congenital anomaly of kidney and urinary tract +  
congenital limb malformation +   
cutis laxa +  
cutis laxa - Marfanoid syndrome 
cysts and fistulae of the face and oral cavity +  
Desbuquois dysplasia +  
developmental anomaly of metabolic origin +  
developmental defect of the eye +   
digestive tract malformation +  
disorder of sexual differentiation +  
Ehlers-Danlos syndrome +  
facial cleft +  
focal dermal hypoplasia 
hemihyperplasia-multiple lipomatosis syndrome 
hereditary hemorrhagic telangiectasia +  
hereditary neurocutaneous angioma 
hydrops fetalis +  
infectious embryofetopathy +  
joint laxity, short stature, and myopia 
Larsen syndrome 
Legius syndrome 
lethal Larsen-like syndrome 
linear nevus sebaceous syndrome 
macroglossia +  
Maffucci syndrome 
marfanoid habitus-inguinal hernia-advanced bone age syndrome 
microtia 
multiple congenital anomalies/dysmorphic syndrome +   
neurofibromatosis type 1 +  
neurofibromatosis-Noonan syndrome +  
nevoid basal cell carcinoma syndrome 
phakomatosis pigmentokeratotica 
phakomatosis pigmentovascularis +  
progeroid syndrome +  
pseudodiastrophic dysplasia 
PTEN hamartoma tumor syndrome +  
schwannomatosis 
toxic or drug-related embryofetopathy +  
TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations +  
urogenital tract malformation +   

Synonyms
Exact Synonyms: Orphanet:83001 ;   http://purl.bioontology.org/ontology/ICD10CM/Q60-Q64
Alternate IDs: MONDO:0019356
Xrefs: GARD:19029 ;   ICD10CM:Q60-Q64 ;   ORDO:83001

paths to the root