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
01846 HMAE anemia, homocystinuria-megaloblastic, cblE complementation type (HMAE) 236270 - 0 0 MTRR - -
01918 HMAG methylcobalamin deficiency, cblG type (HMAG) 250940 - 0 0 MTR - -
02381 NTDFS neural tube defects, folate-sensitive (NTDFS) 601634 - 0 0 MTHFD1, MTHFR, MTR, MTRR - -
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