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
04321 - dysplasia, lymphatic, generalised - - 9 9 PIEZO1 - -
01615 DHS1 stomatocytosis, dehydrated, hereditary, with/without pseudohyperkalemia and/or perinatal edema (DHS, xerocytosis) 194380 AD - - PIEZO1 - -
06293 LMPHM6 Lymphatic malformation 6 616843 AR - - PIEZO1 - -
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