Semmerkrot-Haraldsson-Weenaes syndrome: A very rare syndrome characterized mainly by anemia, missing thumb, an immune disorder and an excessive buildup of fluid in the fetus or newborn (hydrops fetalis). More detailed information about the symptoms, causes, and treatments of Semmerkrot-Haraldsson-Weenaes syndrome is available below.
See full list of 10 symptoms of Semmerkrot-Haraldsson-Weenaes syndrome
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Semmerkrot-Haraldsson-Weenaes syndrome as a "rare disease".
Source - Orphanet
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