Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C1721007
Disease: Pachyonychia Congenita, Type 2 (disorder)
Pachyonychia Congenita, Type 2 (disorder) 		disease 0.780 None 1.000 23 13 1994 2013
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0259771
Disease: Steatocystoma multiplex
Steatocystoma multiplex 		disease 0.750 strong 1.000 7 4 1997 2019
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0265334
Disease: Pachyonychia Congenita
Pachyonychia Congenita 		disease 0.700 None 1.000 13 1 1995 2020
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0037286
Disease: Skin Neoplasms
Skin Neoplasms 		group 0.320 None 1.000 3 0 2015 2018
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		disease 0.310 None 1.000 2 0 2011 2020
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin 		disease 0.300 None 1.000 1 0 2015 2015
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C1368275
Disease: Pigmented Basal Cell Carcinoma
Pigmented Basal Cell Carcinoma 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C3671377
Disease: Sebocystomatosis
Sebocystomatosis 		disease 0.300 None 1.000 1 0 2015 2015
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0263454
Disease: Chloracne
Chloracne 		disease 0.300 None 1.000 1 0 2011 2011
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C1706595
Disease: Pachyonychia Congenita, Jadassohn Lewandowsky Type
Pachyonychia Congenita, Jadassohn Lewandowsky Type 		disease 0.300 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		disease 0.110 None 1.000 1 0 1998 1998
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar 		disease 0.110 None 1.000 1 0 2010 2010
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0014511
Disease: Epithelial cyst
Epithelial cyst 		phenotype 0.110 None 1.000 1 0 2003 2003
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0027651
Disease: Neoplasms
Neoplasms 		group 0.100 None 1.000 15 0 2015 2019
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0033860
Disease: Psoriasis
Psoriasis 		disease 0.100 None 0.929 14 0 2005 2019
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0086543
Disease: Cataract
Cataract 		disease 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0241148
Disease: Cutaneous plaque
Cutaneous plaque 		phenotype 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0038605
Disease: Subungual hyperkeratosis
Subungual hyperkeratosis 		disease 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		phenotype 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0263537
Disease: Onychogryposis
Onychogryposis 		disease 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia 		disease 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C0265319
Disease: Fibrous skin tumor of tuberous sclerosis
Fibrous skin tumor of tuberous sclerosis 		disease 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		phenotype 0.100 None 0 0
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		keratin 17 0.531 0.654 1.1E-11
CUI: C4020960
Disease: Abnormality of nail color
Abnormality of nail color 		disease 0.100 None 0 0