autosomal dominant pseudohypoaldosteronism type 1 (Q32136465)
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pseudohypoaldosteronism characterized by Salt wasting resulting from renal unresponsiveness to mineralocorticoids that has material basis in heterozygous mutation in the NR3C2 gene on chromosome 4q31
- autosomal dominant PHA 1
- PHA1A
Language | Label | Description | Also known as |
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English | autosomal dominant pseudohypoaldosteronism type 1 |
pseudohypoaldosteronism characterized by Salt wasting resulting from renal unresponsiveness to mineralocorticoids that has material basis in heterozygous mutation in the NR3C2 gene on chromosome 4q31 |
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