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General Information
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| Term |
nephrogenic diabetes insipidus type 2 |
ID (Ontology) |
DOID:0081061 (Human Disease) |
| Definition |
A nephrogenic diabetes insipidus that is characterized by the inability of the renal collecting ducts to absorb water in response to antidiuretic hormone and that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding the aquaporin-2 water channel (AQP2), which maps to chromosome 12q13. |
| Also Known As |
"autosomal nephrogenic diabetes insipidus-2" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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nephrogenic diabetes insipidus type 2 | 6 | for disease ribbon | nephrogenic diabetes insipidus type 2 | 6 | model of | nephrogenic diabetes insipidus type 2 | 6 |
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