| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Thrombocytopenia (D013921) |
..Starting node
.. Gardner Morrisson Abbot syndrome (C535643)
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Child Nodes:
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Sister Nodes: |
..Absent radii and thrombocytopenia (C536940)
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..Acquired pure megakaryocytic aplasia (C538176)
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..Congenital amegakaryocytic thrombocytopenia (C535982)
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..Congenital disorder of glycosylation type 1X (C535751)
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..DK Phocomelia Syndrome (C565618)
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..Dyserythropoietic Anemia with Thrombocytopenia (C564525)
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..Evan's syndrome (C536380)
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..FORSYTHE-WAKELING SYNDROME (OMIM:613606)
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..Gardner Morrisson Abbot syndrome (C535643)
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..Giant Platelet Syndrome with Thrombocytopenia (C564237)
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..Glycoprotein IA Deficiency (C566000)
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..Jacobsen Distal 11q Deletion Syndrome (D054868)  1
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..Kasabach-Merritt Syndrome (D059885) 1
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..Macrothrombocytopenia progressive deafness (C537831)
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..Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related (C567747)
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..Macrothrombocytopenia, X-Linked (C564526)
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..MYH9-Related Disorders (C535507)
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..Oculootoradial syndrome (C535544)
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..Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478)
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..Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia (C565328)
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..Spastic Paraplegia And Evans Syndrome (C566652)
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..Tetraphocomelia-Thrombocytopenia Syndrome (C564771)
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..Thrombasthenia-Thrombocytopenia, Hereditary (C566060)
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..Thrombocytopenia 1 (C564052)
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..THROMBOCYTOPENIA 2 (OMIM:188000)
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..Thrombocytopenia 3 (C567487)
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..Thrombocytopenia 4 (C567438)
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..Thrombocytopenia absent ulnar syndrome (C536944)
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..Thrombocytopenia chromosome breakage (C536519)
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..Thrombocytopenia Robin sequence (C536898)
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..Thrombocytopenia with Elevated Serum Iga and Renal Disease (C564051)
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..Thrombocytopenia, cyclic (C536899)
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..Thrombocytopenia, Neonatal Alloimmune (D054098)
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..Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis (C564050)
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..Thrombocytopenia, X-Linked, Intermittent (C564053)
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..THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA (OMIM:300367)
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..Thrombotic Microangiopathies (D057049) 9
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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