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 +     
Chromosome Breakage +     
thrombocytopenia +     
16Q24.3 Microdeletion Syndrome  
6q+ Syndrome, Partial 
7p2 Monosomy Syndrome 
9q22.3 Microdeletion 
Acquired Pure Megakaryocytic Aplasia 
acquired thrombocytopenia +   
Angelman syndrome  
Beckwith-Wiedemann syndrome +   
Braddock Carey Syndrome +   
branchiootorenal syndrome +   
chromosomal duplication syndrome +   
Chromosome 13q-Mosaicism 
Chromosome 22, Monosome Mosaic 
Chromosome 4, 4q Terminal Deletion Syndrome 
Chromosome 6 Ring Syndrome 
Chromosome 7 Ring Syndrome 
Chromosome Deletion +   
congenital amegakaryocytic thrombocytopenia +   
congenital disorder of glycosylation Ix  
Cornelia de Lange syndrome +   
Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities 
deafness, dystonia, and cerebral hypomyelination  
Delayed Cranial Ossification due to CBFB Haploinsufficiency 
Deletion 13q Syndrome, Partial 
Distal Trisomy 10q Syndrome 
DK Phocomelia Syndrome 
Duplication 4p Syndrome 
Edinburgh Malformation Syndrome 
Emanuel Syndrome 
Evans' syndrome +   
Forsythe-Wakeling Syndrome 
Gardner Morrisson Abbot Syndrome 
Giant Platelet Syndrome with Thrombocytopenia  
holoprosencephaly +   
Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type  
Isodicentric Chromosome 15 Syndrome  
Isolated Macrothrombocytopenia +   
IVIC syndrome  
Jacobsen Syndrome +   
Kasabach-Merritt Syndrome +   
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
mosaic variegated aneuploidy syndrome +   
MYH-9 related disease +   
Neonatal Alloimmune Thrombocytopenia  
Pallister Killian Syndrome  
Partial Duplication 15q Syndrome 
Partial Trisomy 3q Syndrome 
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 9  
Prader-Willi syndrome +   
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia +   
Recombinant Chromosome 8 Syndrome  
Rhizomelic Osteochondrodysplasia with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension 
Ring Chromosome 4 Syndrome 
ring chromosome syndrome +   
Schmid-Fraccaro Syndrome  
Sex Chromosome Disorders +   
Silver-Russell syndrome +   
Sotos syndrome +   
Spastic Paraplegia and Evans Syndrome 
Takenouchi-Kosaki Syndrome  
Tetraphocomelia-Thrombocytopenia Syndrome 
Thrombocytopenia 1  
Thrombocytopenia 10  
Thrombocytopenia 11  
Thrombocytopenia 12  
THROMBOCYTOPENIA 13  
Thrombocytopenia 2  
Thrombocytopenia 3  
Thrombocytopenia 4  
Thrombocytopenia 5  
Thrombocytopenia 6  
Thrombocytopenia 7  
Thrombocytopenia 8  
Thrombocytopenia 9  
Thrombocytopenia Absent Ulnar Syndrome 
thrombocytopenia due to platelet alloimmunization +   
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thrombocytopenia, Anemia, and Myelofibrosis  
Thrombocytopenia, Cyclic 
thrombocytopenia-absent radius syndrome  
Thrombotic Microangiopathies +   
transient neonatal thrombocytopenia 
Trisomy 18-Like Syndrome 
Warburton Anyane Yeboa Syndrome  
Warsaw breakage syndrome  
X-linked thrombocytopenia with beta-thalassemia  
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  
XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME  

Synonyms
Exact Synonyms: ANKRD26-RELATED CONDITION ;   Helmerhorst Heaton Crossen syndrome ;   THC2 ;   Thrombocytopenia Chromosome Breakage ;   thrombocytopenia, autosomal dominant ;   thrombocytopenia, autosomal dominant, 2
Xrefs: MESH:C536519 ;   MIM:188000 ;   MONDO:0008555 ;   NCI:C129035

paths to the root