Alagille-Watson syndrome (medical condition): A genetic disorder affecting the liver and characterized by the absence of some or all of the liver bile ducts that transport bile within the liver.
See also:
Alagille Syndrome:
»Introduction: Alagille Syndrome
»Symptoms of Alagille Syndrome
These medical condition or symptom topics may be relevant to medical information for Alagille-Watson syndrome:
Alagille-Watson syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Alagille-Watson syndrome, or a subtype of Alagille-Watson syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Alagille-Watson syndrome: Another name for Alagille Syndrome (or close medical condition association).
»Introduction: Alagille Syndrome
»Symptoms of Alagille Syndrome
Some of the symptoms of Alagille-Watson syndrome incude:
See full list of 55 symptoms of Alagille-Watson syndrome (Alagille Syndrome)
These medical disease topics may be related to Alagille-Watson syndrome:
Source - NIH
Source - CRISP
Search to find out more about Alagille-Watson syndrome:
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