We present extensive magnetic measurements of the (CaxLa1−x)(Ba1.75−xLa0.25+x)Cu3Oy system with its four different families (x) having a T max c (x) variation of 28% and minimal structural changes. For each family, we measured the Néel temperature, the anisotropies of the magnetic interactions, and the spin glass temperature. Our results exhibit a universal relation Tc = cJns for all families, where c ∼ 1, J is the in plane Heisenberg exchange, and ns is the carrier density. This relates cuprate superconductivity to magnetism in the same sense that phonon mediated superconductivity is related to atomic mass.The critical temperature for superconductivity T c in metallic superconductors varies with isotope substitution [1]. This observation, known as the isotope effect, played a key role in exposing their mechanism for superconductivity. In contrast, the mechanism for superconductivity in the cuprate is still elusive, but is believed to be of magnetic origin [2]. Verifying this belief would require an experiment similar to the isotope effect, namely, a measurement of T c versus the magnetic interaction strength J, with no other structural changes in the compounds under investigation. Here we present such an experiment using the (Ca x La 1−x )(Ba 1.75−x La 0.25+x )Cu 3 O y (CLBLCO) system with its four different superconducting families, for which maximum T c (T max c ) varies by 28%. This is a large change compared to Sn, which has the strongest isotope effect in nature where T c varies only by 4%. For each family, we measured the Néel Temperature T N and the anisotropies of the magnetic interactions. This allows us to obtain the Heisenberg coupling J. In addition, we determine the spin glass temperature T g of underdoped samples. J, T g and T c allow us to generate a unified phase diagram for magnetism and superconductivity from no doping to over doping. We combine this result with a previous determination of the superconducting carrier density n s [3], and demonstrate experimentally a magnetic analog of the isotope effect.