All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01090 HSN2C neuropathy, sensory, hereditary, type IIC (HSN-2C) 614213 AR 9 9 KIF1A - -
01091 NESCAVS NESCAV syndrome 614255 AD 8 8 KIF1A - -
01089 SPG30 paraplegia, spastic, type 30, autosomal recessive 610357 AD;AR 5 2 KIF1A - -
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