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Thrombocytopenia 2 (DOID:9003390)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (1) Bonobo: (2) Dog: (2) Squirrel: (1) Pig: (2)
Parent Terms Term With Siblings Child Terms
thrombocytopenia +     
16Q24.3 Microdeletion Syndrome  
6q+ Syndrome, Partial 
7p2 Monosomy Syndrome 
9q22.3 Microdeletion 
Acquired Pure Megakaryocytic Aplasia 
acquired thrombocytopenia +   
Angelman syndrome  
autosomal dominant macrothrombocytopenia TUBB1-related  
Beckwith-Wiedemann syndrome +   
branchiootorenal syndrome +   
chromosomal duplication syndrome +   
Chromosome 13q-Mosaicism 
chromosome 15q13.3 microdeletion syndrome  
chromosome 17p13.3 duplication syndrome  
Chromosome 22, Monosome Mosaic 
Chromosome 3 Duplication Syndrome 
chromosome 3q29 microduplication syndrome 
Chromosome 4, 4q Terminal Deletion Syndrome 
Chromosome 4q- Syndrome 
chromosome 5p13 duplication syndrome 
Chromosome 6 Ring Syndrome 
Chromosome 7 Ring Syndrome 
Chromosome Deletion +   
congenital amegakaryocytic thrombocytopenia  
congenital disorder of glycosylation Ix  
Contiguous Abcd1/Dxs1375e Deletion Syndrome  
Cornelia de Lange syndrome +   
Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities 
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 
Fragile Site 16p12 
Gardner Morrisson Abbot Syndrome 
Giant Platelet Syndrome with Thrombocytopenia 
holoprosencephaly +   
Isodicentric Chromosome 15 Syndrome  
IVIC syndrome  
Jacobsen Syndrome +   
Kasabach-Merritt Syndrome +   
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
Mental Retardation, Fra12a Type  
Monosomy 7 of Bone Marrow 
Mosaic Variegated Aneuploidy Syndrome +   
MYH-9 related disease +   
Neonatal Alloimmune Thrombocytopenia  
NF1 Microduplication Syndrome 
Otodental Dysplasia 
Pallister Killian Syndrome 
Partial Duplication 15q Syndrome 
Partial Trisomy 3q Syndrome 
Patau 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 
Rubinstein-Taybi syndrome +   
Schmid-Fraccaro Syndrome 
Sex Chromosome Disorders +   
Silver-Russell syndrome +   
Smith-Magenis syndrome +   
Sotos syndrome +   
Spastic Paraplegia and Evans Syndrome 
Takenouchi-Kosaki Syndrome  
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 
Trisomy 18-Like Syndrome 
Trisomy 22 Mosaicism Syndrome 
WAGR syndrome +   
Warburton Anyane Yeboa Syndrome 
Warsaw breakage syndrome  
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  

Exact Synonyms: Helmerhorst Heaton Crossen syndrome ;   THC2 ;   Thrombocytopenia Chromosome Breakage ;   Thrombocytopenia, Autosomal Dominant, 2 ;   Thrombocytopenia, autosomal dominant
Primary IDs: MESH:C536519 ;   OMIM:188000 ;   RDO:0015846
Alternate IDs: RDO:0002129

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