All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05861 NEDSWMA;CPSQ1 neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1) 619026 AR 4 4 HPDL - -
00325 SPG paraplegia, spastic (SPG) - - 127 121 AMFR, CAPN1, DDHD2, HPDL, RNF170, SPAST, SPG11, TECPR2, TMEM63C - -
05860 SPG83 paraplegia, spastic, type 83, autosomal recessive (SPG83) 619027 AR 2 2 HPDL - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.