Intracellular signaling of MET and other RTKs occurs via the PI3K or ERK1/2 pathways. Rare mutations and CNVs (which are both designated by ‡) or associated common alleles (which are designated by *) have been identified in individuals with ASD in seven genes encoding proteins involved in these signaling pathways. Of note, an association between common MET variants and ASD has been reported for five independent family cohorts. PLAUR and SERPINE1 associations with ASD have been determined in single, large family cohorts (>600 families). Ras disruption in Smith-Lemli-Opitz syndrome is due to alterations in cholesterol biosynthesis (which is designated by †). Also depicted are other proteins that interact with the MET signaling pathway, such as semaphorins, plexins, and other RTKs. MET can signal via the PI3K and the ERK pathway. RTKs, including MET, are involved in key neurodevelopmental processes, including axon guidance, synapse formation, and plasticity. Convergence of many different genetic etiologies suggests that risk via ERK/PI3K signaling may be common in ASD. Risk, severity of the pathophysiology (i.e., intellectual disability), and disorder heterogeneity may relate to differences in genetic and epigenetic points of entry to the pathways. Thus, the impact due to genetic risk, via regulators of ligand availability or RTKs such as MET, may be less severe than the more severe clinical impact (i.e., intellectual disability) from disruption downstream along the intracellular signaling pathways. c-cbl, E3 ubiquitin-protein ligase c-Cbl; rheb, Ras homolog enriched in brain; RSK, ribosomal S6 kinase; uPA, urokinase plasminogen activator.