Answer:
the disease is dominant and is seen in heterozygous or homozygous dominant individuals
Explanation:
In the question, it was stated that the disease was transferred to two of the children. This shows that the disease is likely a dominant one. In addition, dominant individual with either homozygous or heterozygous alleles will also have the disease. The homozygous individuals usually have two kinds of a similar allele while heterozygous usually have one recessive and one dominant alleles.