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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: LipoDDx: a mobile application for identification of rare lipodystrophy syndromes

Fig. 2

Different screens of LipoDDx®. a First screen. b Screen with dichotomous question. c Screen with a picture of a characteristic sign of some lipodystrophies. d Screen with a drop-down menu for choosing different signs. e Screen of a final results indicating the possible lipodystrophy subtype. In this case, information is given about the genes that should be sequenced and also links to OMIM, and bibliographic references

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