GENETIC ENCYCLOPEDIA
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disease: Infantile histiocytoid cardiomyopathy

id722
nameInfantile histiocytoid cardiomyopathy
variant-disease NM_019056.6(NDUFB11):c.262C>T (p.Arg88Ter) AND Infantile histiocytoid cardiomyopathy
NM_001162529.2(FAM135A):c.474C>G (p.Tyr158Ter) AND Infantile histiocytoid cardiomyopathy
m.15498G>A AND Infantile histiocytoid cardiomyopathy