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
01846 HMAE anemia, homocystinuria-megaloblastic, cblE complementation type (HMAE) 236270 - 0 0 MTRR - -
01918 HMAG methylcobalamin deficiency, cblG type (HMAG) 250940 - 0 0 MTR - -
00139 ID intellectual disability (ID) - - 1837 1570 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
02381 NTDFS neural tube defects, folate-sensitive (NTDFS) 601634 - 0 0 MTHFD1, MTHFR, MTR, MTRR - -
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