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
00215 KRS;CLN12;PARK9 lipofuscinosis, ceroid, neuronal, autosomal recessive,type 4A, Kufs type (CLN-4A), Parkinson disease type 9 (PARK99) 606693 AR 4 4 ATP13A2 - -
06012 SPG78 Spastic paraplegia 78, autosomal recessive 617225 AR 0 0 ATP13A2 - -
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