All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01622 HSAN-2A neuropathy, sensory and autonomic, hereditary, type IIA (HSAN-2A) 201300 - 0 0 WNK1 - -
03666 PHA-2C pseudohypoaldosteronism type 2C (PHA-2C) 614492 - 0 0 WNK1 - -
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