STK11, serine/threonine kinase 11, 6794

N. diseases: 372; N. variants: 145
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0265323
Disease: Peutz-Jeghers polyps of small bowel
Peutz-Jeghers polyps of small bowel
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 1 0.200 None 1.000 6 2002 2008
CUI: C0456487
Disease: Peutz Jehgers polyp
Peutz Jehgers polyp
disease Neoplastic Process 1 0.200 None 1.000 6 2002 2008
CUI: C0406425
Disease: Laugier-Hunziker syndrome
Laugier-Hunziker syndrome
disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C1142307
Disease: Paratubal Cyst
Paratubal Cyst
disease Pathological Conditions, Signs and Symptoms; Neoplasms Disease or Syndrome 1 0.010 None 1.000 1 2012 2012
CUI: C1963822
Disease: Mucosal pigmentation
Mucosal pigmentation
phenotype Sign or Symptom 1 0.010 None 1.000 1 2016 2016
CUI: C0154007
Disease: Benign neoplasm of testis
Benign neoplasm of testis
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 1 0.300 None 0
CUI: C0406814
Disease: Labial lentigo
Labial lentigo
phenotype Neoplasms; Skin and Connective Tissue Diseases; Stomatognathic Diseases Finding 1 0.100 None 0
Neoplasm of uncertain or unknown behavior of testis
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 1 0.300 None 0
Precocious puberty with Sertoli cell tumor
phenotype Endocrine System Diseases Finding 1 0.100 None 0
Abnormal pigmentation of the oral mucosa
phenotype Finding 1 1 0.100 None 0 1
CUI: C4021963
Disease: Lip hyperpigmentation
Lip hyperpigmentation
disease Anatomical Abnormality 1 1 0.100 None 0 1
CUI: C0282207
Disease: Cronkhite-Canada Syndrome
Cronkhite-Canada Syndrome
disease Digestive System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2008 2008
CUI: C1142305
Disease: Melanonychia
Melanonychia
phenotype Finding 2 0.100 None 0
CUI: C2608045
Disease: Trilateral Retinoblastoma
Trilateral Retinoblastoma
disease Neoplasms; Eye Diseases Neoplastic Process 3 1 0.010 None 1.000 1 2013 2013
CUI: C0028433
Disease: Nose Neoplasms
Nose Neoplasms
group Neoplasms; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 3 0.100 None 0
Gastrointestinal hamartomatous polyps
disease Neoplastic Process 4 0.030 None 1.000 3 1999 2004
CUI: C0586737
Disease: Bladder polyp
Bladder polyp
disease Neoplastic Process 4 0.100 None 0
Large cell calcifying Sertoli cell tumor
disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2012 2012
Familial malignant neoplasm of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 5 0.010 None 1.000 1 2004 2004
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation
phenotype Finding 5 2 0.100 None 0 1
CUI: C0206622
Disease: Adenomyoma
Adenomyoma
disease Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2012 2012
CUI: C0744333
Disease: Gastrointestinal polyps
Gastrointestinal polyps
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Neoplastic Process 7 0.070 None 1.000 7 1999 2018
CUI: C1335146
Disease: Osteogenic Neoplasm
Osteogenic Neoplasm
disease Neoplastic Process 7 0.010 None 1.000 1 2019 2019
CUI: C0039747
Disease: Thecoma
Thecoma
disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2005 2005
CUI: C1509148
Disease: Sclerosing hemangioma
Sclerosing hemangioma
disease Neoplastic Process 8 0.010 None 1.000 1 2008 2008