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: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter
phenotype Finding 19 0.100 None 0
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 93 21 0.100 None 0
CUI: C0034888
Disease: Rectal Prolapse
Rectal Prolapse
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 46 1 0.100 None 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
phenotype Finding 59 2 0.100 None 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 53 6 0.100 None 0
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation
phenotype Finding 5 2 0.100 None 0 1
CUI: C0549613
Disease: Biliary tract abnormality
Biliary tract abnormality
phenotype Digestive System Diseases Finding 14 0.100 None 0
Neoplasm of uncertain or unknown behavior of ovary
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 29 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
CUI: C0004509
Disease: Azoospermia
Azoospermia
disease Male Urogenital Diseases Disease or Syndrome 254 70 0.100 None 0
CUI: C0266249
Disease: Gallbladder anomaly congenital
Gallbladder anomaly congenital
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 8 0.100 None 0
CUI: C0347284
Disease: Benign tumor of pancreas
Benign tumor of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 13 0.300 None 0
CUI: C0267373
Disease: Intestinal hemorrhage NOS
Intestinal hemorrhage NOS
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 8 3 0.100 None 0
Abnormal pigmentation of the oral mucosa
phenotype Finding 1 1 0.100 None 0 1
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
Increased level of L-fucose in urine
phenotype Finding 14 0.100 None 0
CUI: C4021963
Disease: Lip hyperpigmentation
Lip hyperpigmentation
disease Anatomical Abnormality 1 1 0.100 None 0 1
CUI: C4024641
Disease: Enlarged polycystic ovaries
Enlarged polycystic ovaries
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 18 0.100 None 0
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm
disease Digestive System Diseases; Neoplasms Neoplastic Process 17 3 0.100 None 0
CUI: C0345832
Disease: Neoplasm of small intestine
Neoplasm of small intestine
disease Digestive System Diseases; Neoplasms Neoplastic Process 9 0.100 None 0
CUI: C0002871
Disease: Anemia
Anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 847 94 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
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.100 None 0 1
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
Malignant Testicular Germ Cell Tumor
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 128 62 0.010 None 1.000 1 1998 1998