Disease Browser
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Parent Node: Heterotaxy Syndrome (D059446) | ..Starting node ..Heterotaxy, Visceral, 3, Autosomal (C565237)
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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: | 5157 |
Name: | Heterotaxy, Visceral, 3, Autosomal |
Definition: | |
Alternative IDs: | OMIM:606325 |
ParentIDs: | MESH:D059446 |
TreeNumbers: | C14.240.400.592/C565237 |C14.280.400.592/C565237 |C15.604.744.146/C565237 |C16.131.077.401/C565237 |C16.131.240.400.592/C565237 |
Synonyms: | HTX3 |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Lymphatic disease |
Reference: |
MedGen: C565237
MeSH: C565237
OMIM: 606325;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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