Ten isolates of Rhizoctonia solani Kuhn (causal agent of Wheat seed decay and seedling damping off diseases) were isolated and identified from the root, soil, and crown of wheat crops (Triticum aestivum L.) in the Qurna and Al-Madina areas of Basrah province، four isolates were obtained from the root zone, three from the crown region, and three from the soil. The isolates exhibited notable morphological and microscopic variation, particularly regarding the number of nuclei, which ranged from 2 to 6.5 per cell, and differing growth rates. The microscopic characteristics analyzed included: hyphal diameter, sclerotia diameter, and Moniloid cell diameter for some isolates, along with the proximity of hyphal septa to constrictions, and the nuclear count. All these factors are crucial in identifying pathogenic isolates. As for the macroscopic characteristics evaluated, these encompassed the color of fungal colonies, their diameter after 72 hours of growth, and the nature of fungal hyphal growth. It was found that multinucleate isolates such as (R2, R3, R4) were more pathogenic and cause a decrease in wheat seed germination rate to 60.00%, compared to control treatment which was 95%. Whereas, the binucleate isolates such as (R6, R7, R8) allowed germination rates exceeding 90% without any significant differences than control. The inhibition efficiency of the fungicide "Topsin-M" (active ingredient: Thiophanate-methyl) against the pathogenic R. solani showed that the highest concentration (2 g/L) inhibited fungal growth by 67.73%, while the lowest concentration (0.5 g/L) resulted in 30.75% inhibition on cultural medium (PDA), with a strong significant correlation between concentration and inhibition rate (correlation coefficient r = 0.98), and an IC₅₀ value of 1.58 g/L. The molecular diagnosis of the pathogenic isolate confirmed 99.403% similarity with R. solani isolates registered in the global GenBank database, under the accession number of PV419663.1.