Nephrosis 1, congenital, Finnish type (medical condition): A rare inherited disorder where the kidney's ability to filter is defective and results in excessive protein in the urine, failure to thrive and malnutrition.
See also:
Finnish nephrosis syndrome:
»Introduction: Finnish nephrosis syndrome
»Symptoms of Finnish nephrosis syndrome
These medical condition or symptom topics may be relevant to medical information for Nephrosis 1, congenital, Finnish type:
Nephrosis 1, congenital, Finnish type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Nephrosis 1, congenital, Finnish type, or a subtype of Nephrosis 1, congenital, Finnish type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Nephrosis 1, congenital, Finnish type: Another name for Finnish nephrosis syndrome (or close medical condition association).
»Introduction: Finnish nephrosis syndrome
»Symptoms of Finnish nephrosis syndrome
Some of the symptoms of Nephrosis 1, congenital, Finnish type incude:
See full list of 8 symptoms of Nephrosis 1, congenital, Finnish type (Finnish nephrosis syndrome)
These medical disease topics may be related to Nephrosis 1, congenital, Finnish type:
Source - NIH
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