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
01845 - homocysteinemia, due to deficiency of MTHFR 236250 - 0 0 MTHFR - -
02381 NTDFS neural tube defects, folate-sensitive (NTDFS) 601634 - 0 0 MTHFD1, MTHFR, MTR, MTRR - -
00212 SCZD schizophrenia (SCZD) 181500 - 51 49 AKT1, APOL2, APOL4, CHI3L1, COMT, DAO, DAOA, DISC1, DISC2, DRD3, DTNBP1, HTR2A, MTHFR, RTN4R - -
01581 THPH-1 thrombophilia (THPH-1) 188050 - 4 3 F13A1, F2, HABP2, MTHFR - -
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