EPC 670A Family Genogram
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EPC 670A Family Genogram

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publish time: 2021-02-28
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Here is a genogram about the EPC 670A family, from which you can see their relationships clearly. The genogram shows the relationship and medical history of a family. It goes beyond traditional genealogy by allowing users to visualize genetic patterns and psychological factors that influence relationships. It can be used to identify repetitive patterns of behavior and identify genetic predispositions. Check more details from this genogram, or learn more in template gallery.

Tags: science

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MITOCHONDRIAL DISORDERS
This kingship diagram is about the mitochondrial disorder.
 MITOCHONDRIAL DISORDERS
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PEDIGREE DIAGRAM SYMBOLS
A pedigree chart shows the presence or absence of a trait or gene through generations within a family. Pedigree charts are used to identify dominant and recessive characteristics. It is used to identify and examine the pattern of inheritance of a specific trait in a lineage.
 PEDIGREE DIAGRAM SYMBOLS
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kingship diagram - x linked dominant
This diagram is about x linked dominant.
 kingship diagram - x linked dominant
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Y linked disorder example
This kinghsip diagram is about y linked disorder.
 Y linked disorder example
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X linked recessive disorder example
This kingship diagram is about x linked recessive disorder.
 X linked recessive disorder example
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Hemophilia Pedigree - Hemophilia Father
Hemophilia is a rare disorder in which your blood doesn't clot normally because it lacks sufficient blood-clotting proteins (clotting factors). Hemophilia is a sex-linked recessive disorder. The gene with the instructions for making factor is found only on the sex chromosome labeled X. This genogram shows the family pedigree when the father is with hemophilia and the mother is normal.
 Hemophilia Pedigree - Hemophilia Father
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Charlotte
Hemophilia Pedigree - Hemophilia Father -Carrier Mother
Hemophilia is a rare disorder in which your blood doesn't clot normally because it lacks sufficient blood-clotting proteins (clotting factors). Hemophilia is a sex-linked recessive disorder. The gene with the instructions for making factor is found only on the sex chromosome labeled X. This genogram shows the family pedigree when the father is with hemophilia and the mother is a carrier.
 Hemophilia Pedigree - Hemophilia Father -Carrier Mother
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Charlotte
Autosomal Recessive Inheritance
In autosomal recessive inheritance, both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. Autosomal recessive disorders are typically not seen in every generation of an affected family. (Refer: U.S. National Library of Medicine)
 Autosomal Recessive Inheritance
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Charlotte
Autosomal Dominant Inheritance
One mutated copy of the gene in each cell is sufficient for a person to be affected by an autosomal dominant disorder. In some cases, an affected person inherits the condition from an affected parent. In others, the condition may result from a new mutation in the gene and occur in people with no history of the disorder in their family. (Refer: U.S. National Library of Medicine)
 Autosomal Dominant Inheritance
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Charlotte
Sex(X)-linked Recessive Inheritance
X-linked recessive disorders are also caused by mutations in genes on the X chromosome. In males (who have only one X chromosome), one altered copy of the gene in each cell is sufficient to cause the condition. In females (who have two X chromosomes), a mutation would have to occur in both copies of the gene to cause the disorder. (Refer: U.S. National Library of Medicine)
 Sex(X)-linked Recessive Inheritance
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Charlotte