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
03812 HSAN9;SPG49 neuropathy, hereditary sensory and autonomic, type IX, with developmental delay (SPG49) 615031 AR - - TECPR2 - -
00325 SPG paraplegia, spastic (SPG) - - 127 121 AMFR, CAPN1, DDHD2, HPDL, RNF170, SPAST, SPG11, TECPR2, TMEM63C - -
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