Table 1.
Historical Classification | Recommended Nomenclature |
---|---|
Niemann–Pick disease type A (NPD A) |
Infantile neurovisceral ASMD (ASMD Type A) |
Intermediate or variant phenotype (NPD A/B) |
Chronic neurovisceral ASMD (ASMD Type A/B) |
Niemann–Pick disease type B (NPD B) |
Chronic visceral ASMD (ASMD Type B) |
ASMD, acid sphingomyelinase deficiency; NPD, Niemann–Pick disease.