Choose correct option.

$(i)$ The heterozygous female transmit the disease to son.

$(ii)$ Change in the shape of the $RBC$ from biconcave disc to elongated sickle like structure.

$(iii)$ Mentally retarded.

$(iv)$ Heamoglobin not formed proper amount in blood.

  • A

    Colour blindness, thalassaemia, pheny ketonuria, anaemia.

  • B

    Haemophilia, sickle cell anaemia,Klinefelter's syndrome, thalassemia.

  • C

    Down's syndrome, klinefelter's syndrome,colour blindness, turner's syndrome. .

  • D

    Haemophilia, sickle cell anaemia,phenyl ketonuria, thalassaemia.

Similar Questions

In the following human pedigree, the filled symbols represent the affected individuals. Identify the type of given pedigree.

  • [NEET 2015]

A woman with two genes for haemophillia and one gene for colourblindness on one of the $X$ chromosomes marries a normal man. How will the progeny be

  • [AIPMT 1998]

An example of a disease of molecular mutation is

The pedigree chart given below shows a particular trait which is absent in parents but present in the next generation irrespective of sexes. Draw your conclusion on the basis of the pedigree.

$A$ : The posssibility of a female becoming a haemophilic is extremely rare.
$R$ : Mother of such a female has to be carrier and father should be haemophilic