Browse result page of "Disorder" of RareLSD

The total number entries retrieved from this search are 8
IDENZYMEGENEEC NUMBERFAMILYCYTOGENETICSDISEASEREFERENCEORGAN
1015AlphacetylglucosaminidaseNAGLU3.2.1.50GH8917q21.2Sanfilippo syndrome type B,CharcotMarieTooth disease9443875, 1376807Nervous System
1024Cathepsin BCTSB3.4.22.1peptidase C18p23.1Keratolytic winter erythema11896452 , 24300638Skin
1028Cathepsin HCTSH3.4.22.16Papain cysteine protease (C1)15q24q25Thyroid crisis,Narcolepsy 1.2587265, 11796715,Nervous System
1030Cathepsin L1CTSL13.4.22.15Papain cysteine protease (C1)9q21q22eccrine acrospiroma,gingival overgrowth9141479 , 8419312 , 8896443Teeth
1031Cathepsin OCTSO3.4.22.42Papain cysteine protease (C1)4q31q32Breast Neoplasms9790772 , 28514442 , 7929457Skin
1032Cathepsin SCTSS3.4.22.27Papain cysteine protease (C1)1q21cercarial dermatitis,corneal dystrophy, subepithel...19593952  , 1373132Eye
1048Legumain (Asparaginyl Endopeptidase)LGMN3.4.22.34peptidase C1314q32.12Schistosomiasis9821970, 9065484, 25630877Schistosomiasis (katayama fever)
1064Thiol reductase, ginterferon inducibleIFI301.8.-.-GILT19p13.11atrophic rhinitis10639150, 10852914, 3136170Nose