Disease | n syndrome |
Phenotype | C0016085|filariasis |
Sentences | 1 |
PubMedID- 25861232 | This syndrome should be diagnosed properly and early and differentiated from similar-looking conditions such as parkes–weber syndrome (pws), lymphatic filariasis, beckwith–wiedemann syndrome, proteus syndrome, russell–silver syndrome, maffucci syndrome, child syndrome (congenital hemidysplasia with ichthyosiform erythroderma and limb defects), neurofibromatosis type 1 (nf1), and triploid syndrome. |
Page: 1