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
03237 ALL leukemia, lymphoid, acute (ALL) 613065 - 7 7 BAX, BCR, FLT3, NBN, NUP214, TAL1, TAL2 - -
02823 anemia anemia, aplastic, incl. susceptibility to 609135 - 46 46 IFNG, NBN, PRF1, SBDS - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00932 NBS Nijmegen breakage syndrome (NBS) 251260 AR 16 15 NBN - cognitive delay; growth retardation; neuropsychiatric behaviors; microcephaly; craniofacial dysmorphia; cleft/arched palate; syndactyly; organ abnormalitie; no cardiac defects; limb reductions; no hearing loss; skin pigmentation abnormalities; elevated cancer incidence; no bone marrow/hematopoietic defects
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