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| Term | visceral heterotaxy 5 | ID (Ontology) | DOID:758 (Human Disease) |
| Definition | A visceral heterotaxy that is characterized by complete right-to-left reversal of the position of the major thoracic and abdominal organs and that has_material_basis_in heterozygous mutation in the NODAL gene on chromosome 10q22. | ||
| Also Known As | "Complete transposition" ; "Laterality sequence" ; "situs inversus" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ physical disorder | |__visceral heterotaxy_________| visceral heterotaxy 5 2 rec. |
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| Is a |
visceral heterotaxy autosomal dominant disease |
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External Crossreferences & Linkouts
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GARD:4883 ICD10CM:Q89.3 ICD9CM:759.3 MESH:D012857 MIM:270100 NCI:C87121 SNOMEDCT_US_2023_03_01:157033002 UMLS_CUI:C0037221 |
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