Orphanet


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Or´phan`et


n.1.A little orphan.
Webster's Revised Unabridged Dictionary, published 1913 by G. & C. Merriam Co.
References in periodicals archive ?
In the differential diagnosis of Peters plus syndrome, similar syndromes such as SHORT, Abbruzo-Erickson, GMS, Weill-Marchesani, Michels, Rieger, Walker-Warburg, Cornelia de Lange, Robinow, and fetal alcohol syndrome can be detected according to Orphanet data (http:77www.orpha.net).
Sainte-Rose, "Craniopharyngioma," Orphanet Journal of Rare Diseases, vol.
Hoffmann, "Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome," Orphanet Journal of Rare Diseases, vol.
Baran, "Yellow nail syndrome: a review," Orphanet Journal of Rare Diseases, vol.
Mahr, Wegener's Granulomatosis Orphanet Encyclopedia, 2004, http://www.orpha.net/data/patho/GB/ukWG.pdf.
Klein-Franke et al., "Gastric lactobezoar --a rare disorder?," Orphanet Journal of Rare Diseases, vol.
El-Hattab, "Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management," Orphanet Journal of Rare Diseases, vol.
De Serres, "Efficacy of alpha-1-antitrypsin augmentation therapy in conditions other than pulmonary emphysema," Orphanet Journal of Rare Diseases, vol.
Wu, "Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing," Orphanet Journal of Rare Diseases, vol.
The findings were published in Orphanet Journal of Rare Diseases.