Disease Browser
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Parent Node: Heterotaxy Syndrome (D059446) | ..Starting node ..Polyasplenia (C566862)
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Sister Nodes: | ..Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome (C565249)
| ..Heterotaxy, Visceral, 3, Autosomal (C565237)
| ..Heterotaxy, visceral, X-linked (C538116)
| ..Heterotaxy, Visceroatrial, Autosomal Recessive (C566864)
| ..Laterality Defects, Autosomal Dominant (C563391)
| ..Left-Right Axis Malformations (C566610)
| ..Polyasplenia (C566862)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 9054 |
Name: | Polyasplenia |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D059446 |
TreeNumbers: | C14.240.400.592/C566862 |C14.280.400.592/C566862 |C15.604.744.146/C566862 |C16.131.077.401/C566862 |C16.131.240.400.592/C566862 |
Synonyms: | Asplenia with Cardiovascular Abnormalities |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Lymphatic disease |
Reference: |
MedGen: C566862
MeSH: C566862
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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