Browse result page of "Disorder" of RareLSD

The total number entries retrieved from this search are 8
IDENZYMEGENEEC NUMBERFAMILYCYTOGENETICSDISEASEREFERENCEORGAN
1024Cathepsin BCTSB3.4.22.1peptidase C18p23.1Keratolytic winter erythema11896452 , 24300638Skin
1025Cathepsin CCTSC3.4.14.1peptidase C111q14.1q14.3Papillon-Lefevre syndrome (PLS)9092576 , 7649281Teeth ,Skin,Nervous System
1026Cathepsin DCTSD3.4.23.5peptidase A1 (Aspartic Protease)11-p15.5NCL(CLN10)10856224, 19159210Nervous System,Lungs,Eye,Muscle,Boness,Head,Nose
1039gammaGlutamyl hydrolaseGGH3.4.19.9peptidase C268q12.23q13.1Tropical Sprue & Methotrexate Toxicity11005824, 5500927  , 10739875Liver
1048Legumain (Asparaginyl Endopeptidase)LGMN3.4.22.34peptidase C1314q32.12Schistosomiasis9821970, 9065484, 25630877Schistosomiasis (katayama fever)
1057ProXaa carboxypeptidasePRCP3.4.16.2peptidase S2811q14.1Sarcoidosis6366093, 230518Lungs,Eye,Skin,HEart
1058Protective protein (cathepsin A)CTSA3.4.16.5peptidase S1020q13.12Galactosialidosis23915561, 6812049, 19097920Nervous System,Boness,Skin,HEart,Ear
1065Tripeptidylpeptidase ITPPI3.4.14.9peptidase S53 domain11-p15.4Neuronal Ceroid Lipofuscinosis2,Autosomal Recessive9653647, 23418007Eye,Nervous System