Disorder inherited as Mendel's law of inheritance called
Mendelian disorder
Chromosomal disorder
Maternal inheritance
Polygenic inheritance
Which of the following diseases belongs to the same category as colourblindness in man
Haemolytic jaundice is caused due to a dominant gene but only $10\%$ of the people actually develop the disease. A heterozygous man marries a homozygous normal woman; what proportion of the children would be expected to develop the haemolytic disease
$A$ : Sickel cell anaemia occurs due to the point mutation.
$R$ : $mRNA$ produced from $Hb(s)$ gene has $GAG$ instead of $GUG$.
Colour blindness is a disease usually affecting man but the factor for it is transmitted to the children always by woman. This is because particular factor is located on