APC, APC regulator of WNT signaling pathway, 324

N. diseases: 703; N. variants: 681
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: C0034882
Disease: Rectal Diseases
Rectal Diseases
group Digestive System Diseases Disease or Syndrome 1 3 0.010 None 1.000 1 2010 2010
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms
group Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 1 0.010 None 1.000 1 2018 2018
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 1 0.010 None 1.000 1 2018 2018
CUI: C0241060
Disease: Cyst of skin
Cyst of skin
disease Pathological Conditions, Signs and Symptoms; Neoplasms Disease or Syndrome 1 0.010 None 1.000 1 1997 1997
CUI: C0333372
Disease: Abscess cavity
Abscess cavity
disease Pathological Conditions, Signs and Symptoms Anatomical Abnormality 1 0.010 None 1.000 1 2019 2019
CUI: C1335749
Disease: Renal Pelvis Carcinoma
Renal Pelvis Carcinoma
disease Neoplastic Process 1 0.010 None 1.000 1 2018 2018
CUI: C1519703
Disease: Turcot Syndrome Type 2
Turcot Syndrome Type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nervous System Diseases Neoplastic Process 1 0.010 None < 0.001 1 2006 2006
CUI: C3665800
Disease: Streptococcal endocarditis
Streptococcal endocarditis
disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4282032
Disease: Senile hyperkeratosis
Senile hyperkeratosis
disease Neoplastic Process 1 0.010 None 1.000 1 2004 2004
CUI: C4744430
Disease: Recurrent Desmoid-Type Fibromatosis
Recurrent Desmoid-Type Fibromatosis
disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 2009 2009
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 1 0.100 None 0
BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 1 2 0.100 None 0 2
ADENOMATOUS POLYPOSIS COLI WITH CONGENITAL CHOLESTEATOMA
disease Finding 1 1 0.100 None 0 1
FAMILIAL ADENOMATOUS POLYPOSIS 1, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C4021146
Disease: Hyperpigmentation of the fundus
Hyperpigmentation of the fundus
phenotype Finding 1 0.100 None 0
CUI: C1851124
Disease: Desmoid disease, hereditary
Desmoid disease, hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 2 11 0.640 strong 1.000 4 11 1996 2011
CUI: C0206646
Disease: Fibromatosis, Abdominal
Fibromatosis, Abdominal
disease Neoplasms Neoplastic Process 2 0.310 None 1.000 2 1997 2000
CUI: C4331965
Disease: Medulloblastoma, WNT-Activated
Medulloblastoma, WNT-Activated
disease Neoplastic Process 2 0.020 None 1.000 2 2018 2019
CUI: C0334558
Disease: Malignant odontogenic tumor
Malignant odontogenic tumor
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 2 0.010 None 1.000 1 2009 2009
CUI: C1859309
Disease: Syndactyly Cenani Lenz type
Syndactyly Cenani Lenz type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 2 9 0.310 None 1.000 1 2015 2015
CUI: C4054287
Disease: Ovarian Microcystic Stromal Tumor
Ovarian Microcystic Stromal Tumor
disease Neoplastic Process 2 0.010 None 1.000 1 2015 2015
CUI: C4324551
Disease: Adrenal nodule
Adrenal nodule
disease Disease or Syndrome 2 0.010 None 1.000 1 2016 2016
CUI: C1707251
Disease: Cancer Other
Cancer Other
disease Neoplastic Process 2 2 0.100 None 0 1
Desmoid Tumor Caused By Somatic Mutation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 2 1 0.300 None 0
CUI: C4025069
Disease: Multiple unerupted teeth
Multiple unerupted teeth
phenotype Stomatognathic Diseases Finding 2 0.100 None 0