Congenital disorders: Difference between revisions

@@ Line 156: / Line 156: @@
 |-
 ||Codominant	|| •Two different versions (alleles) of a gene are expressed.
-•Both alleles influence the genetic trait or determine the characteristics of the genetic condition. ||	ABO blood group, alpha-1 antitrypsin deficiency
+•Both alleles influence the genetic trait or determine the characteristics of the genetic condition.
+||	ABO blood group, alpha-1 antitrypsin deficiency
 |-
 |Mitochondrial	||•Also known as maternal inheritance,
 •Applies to the genes in mitochondrial DNA
-•As only egg cells contribute mitochondria to the developing embryo, only females can pass on mitochondrial mutations to their children.	||Leber hereditary optic neuropathy (LHON)
+•As only egg cells contribute mitochondria to the developing embryo, only females can pass on mitochondrial mutations to their children.
+||Leber hereditary optic neuropathy (LHON)
 |}