It is argued that, in addition to investigations of life span paramete
rs, a large number of biomedically important phenotypes can be profita
bly studied from a gerontological perspective. These would include ''p
rivate'' patterns of aging, especially in our own species, which exhib
its extraordinary genetic heterogeneity. These, as well as a number of
relatively common age-associated phenotypes, have been comparatively
neglected by the gerontological community, and therefore warrant the d
esignation as ''orphan'' phenotypes. From a tabulation of examples fro
m each of the major body systems, five are elaborated upon: ''hyperhip
pocampals,'' defined as individuals with intrinsically enhanced functi
onal reserve in relevant neural circuitry; patients with a heterogeneo
us set of pathologies collectively referred to as ''normal pressure hy
drocephalus''; patients with late life activation of herpes zoster; in
dividuals with unusually early onset of loss of olfactory function; an
d geriatric subjects with unusual sensitivity to ''jet lag.''