All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01581 - Thrombophilia 188050 - - - F13A1, F2, HABP2, MTHFR - -
01845 - homocysteinemia, due to deficiency of MTHFR 236250 - - - MTHFR - -
02381 NTDFS neural tube defects, folate-sensitive (NTDFS) 601634 - - - MTHFD1, MTHFR, MTR, MTRR - -
00212 SCZD schizophrenia (SCZD) 181500 - - - AKT1, APOL2, APOL4, CHI3L1, COMT, DAO, DAOA, DISC1, DISC2, DRD3, DTNBP1, HTR2A, MTHFR, RTN4R - -
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