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: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 539 19 0.500 None 0 1
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
Neoplasm of uncertain or unknown behavior of testis
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 1 0.300 None 0
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: 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: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation
phenotype Finding 5 2 0.100 None 0 1
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 122 24 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: C0151544
Disease: Gastrointestinal carcinoma
Gastrointestinal carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 26 3 0.100 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: 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: C1328931
Disease: Multiple lentigines
Multiple lentigines
disease Disease or Syndrome 13 12 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: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 93 21 0.100 None 0
CUI: C0149651
Disease: Clubbing
Clubbing
phenotype Sign or Symptom 32 1 0.100 None 0
Precocious puberty with Sertoli cell tumor
phenotype Endocrine System Diseases Finding 1 0.100 None 0
CUI: C0039538
Disease: Teratoma
Teratoma
disease Neoplasms Neoplastic Process 171 8 0.100 None 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 725 80 0.100 None 0
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
group Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 32 1 0.100 None 0 1
CUI: C1853237
Disease: Isolated cases
Isolated cases
phenotype Finding 111 0.100 None 0
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 947 45 0.100 None 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
phenotype Finding 59 2 0.100 None 0
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.100 None 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers
disease Musculoskeletal Diseases Anatomical Abnormality 88 1 0.100 None 0
CUI: C0008497
Disease: Choriocarcinoma
Choriocarcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 431 2 0.100 None 0