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
06652 CMT2W Charcot-Marie-Tooth disease, axonal, type 2W 616625 AD - - HACE1 - -
06691 SPPRS Spastic paraplegia and psychomotor retardation with or without seizures 616756 AR - - HACE1 - -
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