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Answer:
recessive
Explanation:
The inheritance pattern of the congenital enzyme deficiency form of the disease is autosomal recessive. Hb M is inherited in an autosomal dominant pattern. There is no association between sex and the frequency of congenital methemoglobinemia.
Methemoglobinemia is an autosomal recessive congenital disorder. It means that both copies of the gene are found to be recessive in order to express a phenotype.
The Dominant trait may be defined as a form of trait which governs by the presence of at least one dominant copy of that gene.
Methemoglobinemia may be defined as a blood disorder in which very little amount of oxygen is delivered to your cells. Cells may feel the scarcity of oxygen.
If an individual is affected by this disorder, both the copies of its gene are found in a recessive form in order to mask the effect of a dominant copy.
Therefore, it is well described above.
To learn more about Methemoglobinemia, refer to the link:
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