STK11, serine/threonine kinase 11, 6794

N. diseases: 231; N. variants: 115
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: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 152 2 0.100 0
Precocious puberty with Sertoli cell tumor
phenotype Finding 1 0.100 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
phenotype Finding 48 0.100 0
CUI: C1842408
Disease: increased risk of pancreatic cancer
increased risk of pancreatic cancer
phenotype Finding 11 0.100 0
CUI: C0018055
Disease: Gonadal Dysgenesis, Mixed
Gonadal Dysgenesis, Mixed
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 26 0.100 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 41 5 0.100 0
CUI: C0034888
Disease: Rectal Prolapse
Rectal Prolapse
disease Digestive System Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 12 1 0.100 0
CUI: C0267373
Disease: Intestinal hemorrhage NOS
Intestinal hemorrhage NOS
phenotype Disease or Syndrome 3 0.100 0
CUI: C0347284
Disease: Benign tumor of pancreas
Benign tumor of pancreas
disease Neoplastic Process 13 0.300 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines
disease Disease or Syndrome 11 1 0.100 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
phenotype Digestive System Diseases; Pathological Conditions, Signs and Symptoms Pathologic Function 60 0.100 0
CUI: C0687713
Disease: Gastrointestinal pain
Gastrointestinal pain
phenotype Sign or Symptom 139 0.100 0
CUI: C0029927
Disease: Ovarian Cysts
Ovarian Cysts
disease Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Neoplasms Disease or Syndrome 74 0.100 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Congenital Abnormality 413 15 0.100 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter
phenotype Finding 7 0.100 0
CUI: C0687149
Disease: Pure gonadal dysgenesis
Pure gonadal dysgenesis
disease Congenital Abnormality 23 0.100 0
CUI: C0036651
Disease: Senile lentigo
Senile lentigo
disease Disease or Syndrome 23 0.100 0
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
disease Hemic and Lymphatic Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 31 6 0.100 0
Abnormality of metabolism/homeostasis
group Finding 154 4 0.100 0
Abnormal pigmentation of the oral mucosa
phenotype Finding 2 0.100 0
CUI: C0154007
Disease: Benign neoplasm of testis
Benign neoplasm of testis
disease Neoplastic Process 1 0.300 0
CUI: C0005424
Disease: Biliary Tract Diseases
Biliary Tract Diseases
group Digestive System Diseases Disease or Syndrome 21 0.100 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers
phenotype Musculoskeletal Diseases Anatomical Abnormality 22 1 0.100 0
Neoplasm of uncertain or unknown behavior of testis
disease Neoplastic Process 1 0.300 0
CUI: C0232487
Disease: Abdominal discomfort
Abdominal discomfort
phenotype Sign or Symptom 137 0.100 0