Phenotypes for disease #01060 (KFSDX (keratosis follicularis spinulosa decalvans, X-linked (KFSDX)), OMIM:308800)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Age/Diagnosis     

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Individual ID     
0000092137 variable phenotype in females correlating with X-inactivation; normal plasma lipid profile; KFSD - - Familial - - - - - Emmelien Aten 00116694
0000092138 KFSD - - Familial - - - - - Emmelien Aten 00116695
0000092139 KFSD - - Familial - - - - - Emmelien Aten 00116696
0000092183 At birth dry, itchy skin, photophobia; at age 4 y corneal dots; at age 8 y widespread follicular hyperkeratosis, red cheeks, and thin eyebrows; hair on scalp appears normal; without family history of KFSD - - Isolated (sporadic) - - - - - Karl-Heinz Grzeschik 00116662
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