Zustand
Holt-oram syndrome
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Varianten, die Holt-oram syndrome basierend auf klinischen Tests beeinflussen
Klinische Testklassifikationen sind darauf ausgelegt, Ärzten dabei zu helfen, zu verstehen, wie genetische Veränderungen, bekannt als Varianten, die Gesundheit einer Person beeinflussen könnten und medizinische Entscheidungen leiten. Varianten werden als Krankheitsverursachend (schädlich), Wahrscheinlich Krankheitsverursachend, Unbekannte Wirkung (unbekannte Auswirkung), Wahrscheinlich Keine Wirkung (wahrscheinlich nicht schädlich) und Keine Wirkung (nicht schädlich) gekennzeichnet. Diese Klassifizierung stützt sich auf eine Mischung aus Familiengeschichte, Labortests und Computerprognosen, um die Auswirkungen der Varianten zu bestimmen.
Varianten, die sowohl biologische Männer als auch Frauen betreffen
Genotype
G
G
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
A
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
A
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C is thought to have no effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Kein Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Unbekannter Effekt
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.