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Agonadism dextrocardia diaphragmatic hernia (medical condition): A very rare syndrome characterized mainly by absent gonads and an underdeveloped right side of the heart.
See also:
Kennerknecht-Sorgo-Oberhoffer syndrome:
»Introduction: Kennerknecht-Sorgo-Oberhoffer syndrome
»Symptoms of Kennerknecht-Sorgo-Oberhoffer syndrome
These medical condition or symptom topics may be relevant to medical information for Agonadism dextrocardia diaphragmatic hernia:
Agonadism dextrocardia diaphragmatic hernia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Agonadism dextrocardia diaphragmatic hernia, or a subtype of Agonadism dextrocardia diaphragmatic hernia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Agonadism dextrocardia diaphragmatic hernia as a "rare disease".
Source - Orphanet
Agonadism dextrocardia diaphragmatic hernia: Another name for Kennerknecht-Sorgo-Oberhoffer syndrome (or close medical condition association).
»Introduction: Kennerknecht-Sorgo-Oberhoffer syndrome
»Symptoms of Kennerknecht-Sorgo-Oberhoffer syndrome
Some of the symptoms of Agonadism dextrocardia diaphragmatic hernia incude:
Source - NIH
Search to find out more about Agonadism dextrocardia diaphragmatic hernia:
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