| Disease Browser
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Parent Node:
 Blood Platelet Disorders (D001791) |
..Starting node
.. Thrombocytopenia (D013921)
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Child Nodes:
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| ........Absent radii and thrombocytopenia (C536940) |
| ........Acquired pure megakaryocytic aplasia (C538176) |
| ........Congenital amegakaryocytic thrombocytopenia (C535982) |
| ........Congenital disorder of glycosylation type 1X (C535751) |
| ........DK Phocomelia Syndrome (C565618) |
| ........Dyserythropoietic Anemia with Thrombocytopenia (C564525) |
| ........Evan's syndrome (C536380) |
| ........FORSYTHE-WAKELING SYNDROME (OMIM:613606) |
| ........Gardner Morrisson Abbot syndrome (C535643) |
| ........Giant Platelet Syndrome with Thrombocytopenia (C564237) |
| ........Glycoprotein IA Deficiency (C566000) |
........Jacobsen Distal 11q Deletion Syndrome (D054868)  1 |
| ........Kasabach-Merritt Syndrome (D059885) 1 |
| ........Macrothrombocytopenia progressive deafness (C537831) |
| ........Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related (C567747) |
| ........Macrothrombocytopenia, X-Linked (C564526) |
| ........MYH9-Related Disorders (C535507) |
| ........Oculootoradial syndrome (C535544) |
| ........Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478) |
| ........Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia (C565328) |
| ........Spastic Paraplegia And Evans Syndrome (C566652) |
| ........Tetraphocomelia-Thrombocytopenia Syndrome (C564771) |
| ........Thrombasthenia-Thrombocytopenia, Hereditary (C566060) |
| ........Thrombocytopenia 1 (C564052) |
| ........THROMBOCYTOPENIA 2 (OMIM:188000) |
| ........Thrombocytopenia 3 (C567487) |
| ........Thrombocytopenia 4 (C567438) |
| ........Thrombocytopenia absent ulnar syndrome (C536944) |
| ........Thrombocytopenia chromosome breakage (C536519) |
| ........Thrombocytopenia Robin sequence (C536898) |
| ........Thrombocytopenia with Elevated Serum Iga and Renal Disease (C564051) |
| ........Thrombocytopenia, cyclic (C536899) |
| ........Thrombocytopenia, Neonatal Alloimmune (D054098) |
| ........Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis (C564050) |
| ........Thrombocytopenia, X-Linked, Intermittent (C564053) |
| ........THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA (OMIM:300367) |
| ........Thrombotic Microangiopathies (D057049) 9 |
Sister Nodes: |
..Bernard-Soulier Syndrome (D001606) 5
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..BLEEDING DISORDER, PLATELET-TYPE, 8 (OMIM:609821)
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..Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality (C565600)
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..Gray Platelet Syndrome (D055652) 1
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..Platelet Aggregation, Spontaneous (C566800)
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..Platelet Disorder, Familial, with Associated Myeloid Malignancy (C563324)
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..Platelet Disorder, Undefined (C566799)
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..Platelet Factor 3 Deficiency (C566798)
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..Platelet Glycoprotein IV Deficiency (C564245)
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..Platelet Prostacyclin Receptor Defect (C564884)
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..Platelet Receptor for Collagen, Deficiency of (C565999)
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..Platelet Signal Processing Defect (C566796)
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..Platelet Storage Pool Deficiency (D010981) 5
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..Primary Release Disorder Of Platelets (C566759)
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..Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet (C567786)
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..Stormorken Syndrome (C566108)
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..Thrombasthenia (D013915) 3
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..Thrombocytopenia (D013921) 48
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..Thrombocytosis (D013922) 4
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..Thromboxane Synthetase Deficiency (C562866)
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..von Willebrand Diseases (D014842) 6
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..White platelet syndrome (C536702)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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