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
chromosomal disease +     
Monosomy +     
16Q24.3 Microdeletion Syndrome  
6q+ Syndrome, Partial 
7p2 Monosomy Syndrome 
9q22.3 Microdeletion 
Angelman syndrome  
Beckwith-Wiedemann syndrome +   
branchiootorenal syndrome +   
chromosomal duplication syndrome +   
Chromosome 13q-Mosaicism 
Chromosome 18 Mosaic Monosomy 
Chromosome 22, Monosome Mosaic 
Chromosome 4, 4q Terminal Deletion Syndrome 
Chromosome 6 Ring Syndrome 
Chromosome 7 Ring Syndrome 
Chromosome Deletion +   
Actual loss of portion of a chromosome.
Cornelia de Lange syndrome +   
deafness, dystonia, and cerebral hypomyelination  
Delayed Cranial Ossification due to CBFB Haploinsufficiency 
Deletion 13q Syndrome, Partial 
Distal Trisomy 10q Syndrome 
Duplication 4p Syndrome 
Edinburgh Malformation Syndrome 
Emanuel Syndrome 
holoprosencephaly +   
Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type  
Isodicentric Chromosome 15 Syndrome  
mosaic variegated aneuploidy syndrome +   
Pallister Killian Syndrome  
Partial Duplication 15q Syndrome 
Partial Trisomy 3q Syndrome 
Prader-Willi syndrome +   
Recombinant Chromosome 8 Syndrome 
Ring Chromosome 4 Syndrome 
Schmid-Fraccaro Syndrome  
Sex Chromosome Disorders +   
Silver-Russell syndrome +   
Sotos syndrome +   
Thrombocytopenia 2  
Trisomy 18-Like Syndrome 
Warburton Anyane Yeboa Syndrome  
 16Q24.3 Microdeletion Syndrome  
 7p2 Monosomy Syndrome 
 chromosomal deletion syndrome +   
 Chromosome 1, Deletion q21 q25 
 Chromosome 1, Monosomy 1p 
 Chromosome 1, Monosomy 1p22 p13 
 Chromosome 1, Monosomy 1p31 p22 
 Chromosome 1, Monosomy 1p32 
 Chromosome 1, Monosomy 1p34 p32 
 Chromosome 1, Monosomy 1q25 q32 
 Chromosome 1, Monosomy 1q32 q42 
 Chromosome 1, Monosomy 1q4 
 Chromosome 10, Monosomy 10q 
 Chromosome 11p, Partial Deletion 
 Chromosome 11q Partial Deletion 
 Chromosome 12p Deletion 
 Chromosome 12p Partial Deletion 
 Chromosome 14q, Partial Deletions 
 Chromosome 14q, Terminal Deletion 
 Chromosome 15q, partial deletion 
 Chromosome 17, Deletion 17q23 q24 
 Chromosome 18, Deletion 18q23 
 Chromosome 2, Monosomy 2p22 
 Chromosome 2, Monosomy 2pter p24 
 Chromosome 2, Monosomy 2q 
 Chromosome 2, Monosomy 2q24 
 Chromosome 20, Deletion 20p 
 Chromosome 21 Monosomy 
 Chromosome 21, Monosomy 21q22 
 Chromosome 22, Microdeletion 22 q11 
 CHROMOSOME 2p16.3 DELETION SYNDROME  
 Chromosome 3, Monosomy 3p 
 Chromosome 3, Monosomy 3p14 p11 
 Chromosome 3, Monosomy 3p2 
 Chromosome 3, Monosomy 3p25  
 Chromosome 3, Monosomy 3q21 23 
 Chromosome 3, Monosomy 3q27 
 Chromosome 4 Short Arm Deletion 
 Chromosome 4, 4q Terminal Deletion Syndrome 
 Chromosome 4, Monosomy 4p14 p16 
 Chromosome 4, Monosomy 4q32 
 Chromosome 4q- Syndrome 
 Chromosome 6, Deletion 6q13 q15 
 Chromosome 6, Monosomy 6p23 
 Chromosome 6, Monosomy 6q 
 Chromosome 6, Monosomy 6q1 
 Chromosome 6, monosomy 6q2 
 Chromosome 7, Monosomy 
 Chromosome 7, Monosomy 7q2 
 Chromosome 7, Monosomy 7q21 
 Chromosome 7, monosomy 7q3 
 Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB  
 Chromosome 8 Deletion +  
 Chromosome 8, Monosomy 8p 
 Chromosome 8, Monosomy 8p23 1 
 Chromosome 8, Monosomy 8q 
 Chromosome 8p Deletion Syndrome (partial) 
 Chromosome 9, Partial Monosomy 9p 
 Deletion 13q Syndrome, Partial 
 Deletion 6q16 q21 
 Generalized Hypertrichosis Terminalis, with or without Gingival Hyperplasia  
 Male Sterility due to Y-Chromosome Deletions 
 Prader-Willi-Like Syndrome Associated with Chromosome 6 
 X Chromosome, Monosomy Xp22 pter 
 X Chromosome, Monosomy Xq28 

Synonyms
Exact Synonyms: Partial Monosomies ;   Partial Monosomy ;   chromosome deletions
Primary IDs: MESH:D002872
Definition Sources: MESH:D002872

paths to the root