Disease Browser
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Parent Node: Chromosome Deletion (D002872) | Parent Node: Chromosome Disorders (D025063) | Parent Node: Leukemia, Myeloid, Acute (D015470) | Parent Node: Myelodysplastic Syndromes (D009190) | ..Starting node ..Monosomy 7 of Bone Marrow (C565370)
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Sister Nodes: | ..Alpha-Thalassemia Myelodysplasia Syndrome (C563023)
| ..Anemia, Refractory (D000753) 2
| ..Anemia, Sideroblastic (D000756) 8
| ..Hemoglobinuria, Paroxysmal (D006457) 2
| ..Monosomy 7 of Bone Marrow (C565370)
| ..Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay (C563345)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 7382 |
Name: | Monosomy 7 of Bone Marrow |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002872|MESH:D009190|MESH:D015470|MESH:D025063 |
TreeNumbers: | C04.557.337.539.275/C565370 |C15.378.190.625/C565370 |C16.131.260/C565370 |C16.320.180/C565370 |C23.550.210.050.500.500/C565370 |
Synonyms: | Myelodysplasia and Leukemia Syndrome with Monosomy 7 |
Slim Mappings: | Blood disease|Cancer|Congenital abnormality|Genetic disease (inborn)|Pathology (process) |
Reference: |
MedGen: C565370
MeSH: C565370
OMIM: 252270;
Genes: AF8T; | Phenotypes | | Disease Causing ClinVar Variants | |
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