WordNet

a way of doing something, especially a systematic way; implies an orderly logical arrangement (usually in steps)
a watch with a hinged metal lid to protect the crystal (同)hunting watch
someone who hunts game (同)huntsman
a person who searches for something; "a treasure hunter"
Englishman and Pre-Raphaelite painter (1827-1910) (同)Holman Hunt, William Holman Hunt
British writer who defended the Romanticism of Keats and Shelley (1784-1859) (同)Leigh Hunt, James Henry Leigh Hunt
United States architect (1827-1895) (同)Richard Morris Hunt

PrepTutorEJDIC

〈C〉(特に秩序だった)(…の)『方法』,方式《+『of』+『名』(do『ing』)》 / 〈C〉〈U〉(思考行・行為・行動の)きちょうめんさ;秩序,筋道
(また『huntsman』)『ハンター』,狩猟家 / 猟八;(特にキツネ狩りの)猟馬 / (…の)追求者;(…を)探求する人《+『for』(『after』)+『名』》

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1. ムコ多糖症：臨床的特徴および診断mucopolysaccharidoses clinical features and diagnosis [show details]
… pearly papular skin lesions over the scapulae and on the lateral upper arms and thighs develop in some Hunter patients . Some patients with the severe form have aggressive hyperactive behavior similar to Sanfilippo … measured in all patients with a suspected MPS. Both a quantitative test of total GAG and a fractionation method, such as electrophoresis or chromatography, to distinguish among the different types of GAGs should …
2. ムコ多糖症：治療mucopolysaccharidoses treatment [show details]
…function and the 12-minute walk test . Intrathecal therapy remains experimental. ERT for MPS II (Hunter syndrome) with recombinant human iduronate sulfatase (idursulfase) is licensed for use in many countries …
3. ムコ多糖症：合併症mucopolysaccharidoses complications [show details]
… disease but often become unresponsive as the disease progresses to its final stages. In severe Hunter (MPS II) and Sanfilippo (MPS III) syndromes, developmental delay typically is noted at two to six years … All MPS patients should be evaluated for carpal tunnel syndrome using standard methods,…
4. 小児の聴覚障害：病因hearing loss in children etiology [show details]
…this type of hearing loss . Among the X-linked disorders associated with SNHL are Hunter syndrome (mucopolysaccharidosis 2), Alport syndrome, X-linked congenital SNHL, and early onset progressive SNHL .…
5. 先天性代謝異常：個々の障害の発見inborn errors of metabolism identifying the specific disorder [show details]
… The testing methods and disorders that are screened vary from state to state and country to country.… autosomal-recessive inheritance, although some, such as ornithine transcarbamylase deficiency, Hunter syndrome, X-linked adrenoleukodystrophy, and creatine transporter deficiency, are X linked and some, …