AR, androgen receptor, 367

N. diseases: 854; N. variants: 163
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: C4024646
Disease: Aplasia/Hypoplasia of the fallopian tube
Aplasia/Hypoplasia of the fallopian tube 		phenotype Finding 2 0.100 None 0
CUI: C0556385
Disease: Craving for alcohol
Craving for alcohol 		phenotype Finding 3 0.300 None 1.000 1 2010 2010
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		disease Nervous System Diseases Disease or Syndrome 3 1 0.010 None 1.000 1 1992 1992
CUI: C1332353
Disease: Atypical Small Acinar Proliferation of the Prostate Gland
Atypical Small Acinar Proliferation of the Prostate Gland 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 3 0.010 None 1.000 1 2019 2019
CUI: C1335409
Disease: Prostate Phyllodes Tumor
Prostate Phyllodes Tumor 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 3 0.010 None 1.000 1 2007 2007
CUI: C1609519
Disease: Myelolipoma of adrenal gland
Myelolipoma of adrenal gland 		disease Neoplastic Process 3 0.010 None 1.000 1 2008 2008
CUI: C2919327
Disease: Pleomorphic lobular carcinoma in situ
Pleomorphic lobular carcinoma in situ 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 3 0.010 None 1.000 1 2009 2009
CUI: C4025825
Disease: Abnormal external genitalia
Abnormal external genitalia 		disease Anatomical Abnormality 3 0.010 None 1.000 1 2011 2011
CUI: C1848182
Disease: Blind vagina
Blind vagina 		disease Congenital Abnormality 3 0.100 None 0
CUI: C1848192
Disease: Absent facial hair
Absent facial hair 		phenotype Congenital Abnormality 3 0.100 None 0
CUI: C1859391
Disease: Absent pubic hair
Absent pubic hair 		phenotype Finding 3 1 0.100 None 0 1
CUI: C2895223
Disease: Juvenile and adolescent idiopathic scoliosis
Juvenile and adolescent idiopathic scoliosis 		disease Musculoskeletal Diseases Anatomical Abnormality 4 0.020 None 1.000 2 2012 2014
CUI: C0563449
Disease: Epispadias, male (disorder)
Epispadias, male (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 4 0.010 None 1.000 1 2010 2010
CUI: C1332139
Disease: Prostate Acinar Adenocarcinoma
Prostate Acinar Adenocarcinoma 		disease Neoplasms Neoplastic Process 4 0.010 None 1.000 1 2019 2019
CUI: C1334615
Disease: Malignant Phyllodes Tumor of Prostate
Malignant Phyllodes Tumor of Prostate 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4 0.010 None 1.000 1 2007 2007
CUI: C1854013
Disease: Anisomastia
Anisomastia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Anatomical Abnormality 4 0.010 None 1.000 1 2017 2017
CUI: C4040907
Disease: Mosaic Turner syndrome
Mosaic Turner syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C0017250
Disease: Psychosexual identity disorder
Psychosexual identity disorder 		group Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2009 2009
CUI: C0038476
Disease: Supernumerary structure
Supernumerary structure 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 5 0.010 None 1.000 1 2005 2005
CUI: C0346013
Disease: Fibroepithelioma of Pinkus
Fibroepithelioma of Pinkus 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2007 2007
CUI: C0346057
Disease: Cutaneous neurofibroma
Cutaneous neurofibroma 		disease Neoplasms; Nervous System Diseases Neoplastic Process 5 1 0.010 None 1.000 1 2019 2019
CUI: C0553647
Disease: calcifying aponeurotic fibroma
calcifying aponeurotic fibroma 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2008 2008
CUI: C2717866
Disease: Vestibulodynia
Vestibulodynia 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 2014 2014
CUI: C3280428
Disease: Alpha-Methylacyl-CoA Racemase Deficiency
Alpha-Methylacyl-CoA Racemase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2017 2017
CUI: C3469524
Disease: PROSTATE CANCER, SUSCEPTIBILITY TO
PROSTATE CANCER, SUSCEPTIBILITY TO 		phenotype Finding 5 6 0.100 None 0 1