Pseudohypoaldosteronism, type ib2, autosomal recessive

Preferred Label : Pseudohypoaldosteronism, type ib2, autosomal recessive;

Symbol : PHA1B2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620125;

Details

Origin ID

620125;

UMLS CUI

C5774255;

Genes related to phenotype
- Sodium channel, epithelial 1, beta subunit [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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