Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

thrombocytopenia-absent radius syndrome (DOID:14699)
Annotations: Rat: (12) Mouse: (12) Human: (13) Chinchilla: (12) Bonobo: (12) Dog: (12) Squirrel: (11) Pig: (12)
Parent Terms Term With Siblings Child Terms
10p Deletion Syndrome (partial) 
16p11.2 Deletion Syndrome  
1q24 Deletion Syndrome  
22q11 Deletion Syndrome +   
3p- syndrome 
Acquired Pure Megakaryocytic Aplasia 
acquired thrombocytopenia +   
autosomal dominant macrothrombocytopenia TUBB1-related  
chromosome 10q23 deletion syndrome  
Chromosome 11p Deletion Syndrome 
chromosome 13q14 deletion syndrome  
chromosome 14q11-q22 deletion syndrome 
chromosome 15q11.2 deletion syndrome  
chromosome 15q13.3 microdeletion syndrome  
chromosome 15q24 deletion syndrome  
chromosome 15q25 deletion syndrome 
chromosome 15q26-qter deletion syndrome 
chromosome 16p11.2 deletion syndrome, 220kb 
chromosome 16p12.1 deletion syndrome, 520kb 
chromosome 16p12.2-p11.2 deletion syndrome 
chromosome 16q22 deletion syndrome 
chromosome 17p13.1 deletion syndrome 
chromosome 17q11.2 deletion syndrome, 1.4Mb  
chromosome 17q12 deletion syndrome  
chromosome 17q23.1-q23.2 deletion syndrome 
chromosome 18p deletion syndrome 
chromosome 18q deletion syndrome  
chromosome 19p13.13 deletion syndrome 
chromosome 19q13.11 deletion syndrome 
chromosome 1p32-p31 deletion syndrome  
chromosome 1p36 deletion syndrome  
chromosome 1q21.1 deletion syndrome  
chromosome 1q41-q42 deletion syndrome +   
chromosome 22q11.2 deletion syndrome, distal  
chromosome 2p12-p11.2 deletion syndrome 
chromosome 2p16.1-p15 deletion syndrome 
chromosome 2q31.2 deletion syndrome 
chromosome 2q32-q33 deletion syndrome  
chromosome 3q13.31 deletion syndrome 
chromosome 3q29 microdeletion syndrome 
chromosome 4q21 deletion syndrome 
chromosome 5q12 deletion syndrome 
chromosome 6pter-p24 deletion syndrome 
chromosome 6q11-q14 deletion syndrome 
chromosome 6q24-q25 deletion syndrome 
chromosome 8q21.11 deletion syndrome 
chromosome 9p deletion syndrome  
chromosome Xp21 deletion syndrome 
congenital amegakaryocytic thrombocytopenia  
congenital disorder of glycosylation Ix  
Congenital Hand Deformities +   
Cri-du-Chat syndrome +   
Cubitus Valgus with Mental Retardation and Unusual Facies 
distal 10q deletion syndrome 
DK Phocomelia Syndrome 
Evans' syndrome +   
Forsythe-Wakeling Syndrome 
Fryns Hofkens Fabry Syndrome 
Gardner Morrisson Abbot Syndrome 
Giant Platelet Syndrome with Thrombocytopenia 
Holt-Oram syndrome  
Hypomelia Mullerian Duct Anomalies 
hypoparathyroidism-deafness-renal disease syndrome  
IVIC syndrome  
Jacobsen Distal 11q Deletion Syndrome +   
Kasabach-Merritt Syndrome +   
Kleefstra syndrome +   
Koolen de Vries syndrome  
Miller-Dieker lissencephaly syndrome  
MYH-9 related disease +   
Neonatal Alloimmune Thrombocytopenia  
Ophthalmomandibulomelic Dysplasia 
Phelan-McDermid syndrome  
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 9  
Potocki-Shaffer Syndrome 
Radio Renal Syndrome 
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia +   
Rhizomelic Osteochondrodysplasia with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension 
Smith-Magenis syndrome +   
Spastic Paraplegia and Evans Syndrome 
Takenouchi-Kosaki Syndrome  
Tamari Goodman Syndrome 
Terminal Transverse Defects of Arm 
Tetraphocomelia-Thrombocytopenia Syndrome 
Thrombocytopenia 1  
Thrombocytopenia 2  
Thrombocytopenia 3  
Thrombocytopenia 4  
Thrombocytopenia Absent Ulnar Syndrome 
thrombocytopenia due to platelet alloimmunization +   
Thrombocytopenia Robin Sequence 
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thrombocytopenia, Anemia, and Myelofibrosis  
Thrombocytopenia, Cyclic 
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis  
thrombocytopenia-absent radius syndrome  
Thrombotic Microangiopathies +   
transient neonatal thrombocytopenia 
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
WAGR syndrome +   
Williams-Beuren syndrome +   
Wolf-Hirschhorn syndrome  
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  

Exact Synonyms: Absent Radii and Thrombocytopenia ;   Chromosome 1q21.1 Deletion Syndrome, 200-Kb ;   Radial Aplasia-Amegakaryocytic Thrombocytopenia ;   Radial Aplasia-Thrombocytopenia Syndrome ;   TAR ;   TAR Syndrome ;   Thrombocytopenia Absent Radii ;   Thrombocytopenia with absent radii (TAR) syndrome ;   chromosome 1q21.1 deletion syndrome
Primary IDs: MESH:C536940 ;   RDO:0002669
Alternate IDs: OMIM:274000
Xrefs: NCI:C99038 ;   ORDO:3320

paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.