Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
retinitis pigmentosa 6
MONDO:0000910
Brunner syndrome
MONDO:0010379
X-linked lymphoproliferative disease due to XIAP deficiency
MONDO:0010385
blue cone monochromacy
MONDO:0010563
X-linked dominant hypophosphatemic rickets
MONDO:0010619
recessive X-linked ichthyosis
MONDO:0010622