Browse result page of "Disorder" of RareLSD

The total number entries retrieved from this search are 8
IDENZYMEGENEEC NUMBERFAMILYCYTOGENETICSDISEASEREFERENCEORGAN
1027Cathepsin FCTSF3.4.22.41Papain cysteine protease(C1)11q13.1q13.3Adult Onset Ceroid lipofuscinosis (Ceroid Lipofuscinosis, Neuronal, 13, Kufs Type)23297359Nervous System
1028Cathepsin HCTSH3.4.22.16Papain cysteine protease (C1)15q24q25Thyroid crisis,Narcolepsy 1.2587265, 11796715,Nervous System
1029Cathepsin KCTSK3.4.22.38Papain cysteine protease (C1)1q21Pycnodysostosis (PKND)1049121 , 125731710Head,Nose,Teeth,,Boness,Skin,Hair
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
1033Cathepsin VCTSV3.4.22.43Papain cysteine protease (C1)9q22.2NA10029531 , 11027133 , 9727401NA
1034Cathepsin ZCTSZ3.4.18.1Papain cysteine protease (C1)20q13.32dacryoadenitis9642240 , 18420963, 10653163NA