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RIDDLE Syndrome
(OMIM ID: 611943)


Human immunodeficiency syndrome characterised by immunoglobulin deficiency, learning difficulties, dysmorphic facial features and a hypersensitivity to ionising radiation. Reduced head size and ataxia may also be features of the disease


Following keywords are related to RIDDLE Syndrome:

Last modification of this entry: Nov. 11, 2010.

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