All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01242 - dementia, familial, Danish 117300 AD - - ITM2B - -
01522 - dementia, familial, British 176500 AD - - ITM2B - -
04528 RDGCA dystrophy, retinal?, with inner retinal dysfunction and ganglion cell abnormalities (RDGCA) 616079 AD - - ITM2B - -
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