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
00324 CP palsy, cerebral (CP) - - 5 5 AP4M1 - -
03211 SPG50; CPSQ3 paraplegia, spastic, autosomal recessive, type 50 (SPG-50, cerebral palsy, spastic quadriplegic, type 3 (CPSQ-3)) 612936 AR 1 - AP4M1 - -
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