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: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0575157
Disease: Deformity of spine
Deformity of spine
disease 0.010 None 1.000 1 0 2007 2007
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
disease 0.010 None 1.000 1 0 2013 2013
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0334583
Disease: Pilocytic Astrocytoma
Pilocytic Astrocytoma
disease 0.010 None 1.000 1 0 2002 2002
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0278502
Disease: recurrent gastric cancer
recurrent gastric cancer
disease 0.010 None 1.000 1 0 2017 2017
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0271683
Disease: Polyneuropathy, Motor
Polyneuropathy, Motor
disease 0.010 None 1.000 1 0 2001 2001
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
disease 0.010 None 1.000 1 1 2011 2011
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
Charcot-Marie-Tooth disease, Type 1C
disease 0.010 None 1.000 1 0 2017 2017
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0267375
Disease: Chronic colitis
Chronic colitis
disease 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
disease 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0262576
Disease: Nerve paralysis
Nerve paralysis
disease 0.010 None 1.000 1 0 2014 2014
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease 0.010 None 1.000 1 0 2017 2017
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0376544
Disease: Hematopoietic Neoplasms
Hematopoietic Neoplasms
group 0.010 None 1.000 1 0 2004 2004
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0522224
Disease: Paralysed
Paralysed
phenotype 0.010 None 1.000 1 0 2004 2004
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
phenotype 0.010 None 1.000 1 0 2017 2017
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0494491
Disease: Mononeuropathies
Mononeuropathies
group 0.010 None 1.000 1 0 2014 2014
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0476273
Disease: Respiratory distress
Respiratory distress
phenotype 0.010 None 1.000 1 0 2011 2011
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized
phenotype 0.010 None 1.000 1 0 2000 2000
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0432470
Disease: 46, XY female
46, XY female
disease 0.010 None 1.000 1 0 2004 2004
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
Steroid-sensitive nephrotic syndrome
disease 0.010 None 1.000 1 0 2019 2019
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0242287
Disease: Isaacs syndrome
Isaacs syndrome
disease 0.010 None 1.000 1 0 1999 1999
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
disease 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
Muscular Dystrophy, Facioscapulohumeral
disease 0.010 None 1.000 1 0 2013 2013
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
peripheral myelin protein 22 0.471 0.885 0.91
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx
disease 0.010 None < 0.001 1 0 2017 2017