Given below is a pedigree chart showing the inheritance of a certain diseases :
Identify the type of the disease.

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The pedigree chart shows inheritance of a disease across generations. We observe that affected individuals (filled symbols) appear in every generation, and both males and females are affected.
Since both males and females are affected, the disease is not Y-linked (only males would be affected) and likely not X-linked dominant (which would show no male-to-male transmission). Here, there is male-to-male transmission (e.g., affected father passing to son), which rules out X-linked inheritance. Thus, the disease is autosomal.
Affected individuals appear in every generation, and every affected child has at least one affected parent. This pattern is characteristic of an autosomal dominant disorder. In autosomal recessive disorders, affected individuals may not appear in every generation, and affected children can have unaffected parents.
The disease is Autosomal dominant.
For autosomal dominant inheritance, if one parent is heterozygous affected (Aa) and the other is unaffected (aa), the probability of an affected child is:
For autosomal recessive inheritance, if both parents are carriers (Aa), the probability of an affected child (aa) is: