All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03373 HSAN-1C neuropathy, sensory and autonomic, hereditary, type IC (HSAN-1C) 613640 - 0 0 SPTLC2 - -
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