All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00383 NS Noonan syndrome (NS) - - 232 225 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2, SPRED2 - autosomal dominant
05855 NS10 Noonan syndrome, type 10 (NS10) 616564 AD - - LZTR1 - -
05854 NS2 Noonan syndrome, type 2 (NS2) 605275 AR 1 1 LZTR1 - -
05389 SWNTS Schwannomatosis (SWNTS) - - 89 88 LZTR1, NF2, SMARCB1 - -
00437 SWNTS2 Schwannomatosis, type 2 (SWNTS2) 615670 AD 2 2 LZTR1 - -
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