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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease congenital ichthyosiform erythroderma
Comorbidity C0008445|chondrodysplasia punctata
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PubMedID- 20929975 Herein, we will review clinical and basic science aspects of smith-lemli-opitz syndrome, desmosterolosis, lathosterolosis, hem dysplasia, x-linked dominant chondrodysplasia punctata, congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome, sterol-c-4 methyloxidase-like deficiency, and antley-bixler syndrome.

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