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inherited acute myeloid leukemia

Disease Summary
Associated Targets (2)
Tclin

2


Explore Associated Targets
Mondo Description An instance of acute myeloid leukemia that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0017893:  inherited acute myeloid leukemia
Orphanet:319465: 
SCTID:764940002: 
UMLS:CN203946: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found