Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
X-linked intellectual disability-retinitis pigmentosa syndrome
MONDO:0010364
Xp22.3 microdeletion syndrome
MONDO:0015606
atypical Norrie disease due to monosomy Xp11.3
MONDO:0016850
glycerol kinase deficiency, infantile form
MONDO:0017294
isolated glycerol kinase deficiency
MONDO:0018459