VSX1, visual system homeobox 1, 30813

N. diseases: 95; N. variants: 18
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: C0221074
Disease: Depression, Postpartum
Depression, Postpartum
disease Female Urogenital Diseases and Pregnancy Complications; Mental Disorders Mental or Behavioral Dysfunction 54 6 0.010 None 1.000 1 2019 2019
CUI: C0220769
Disease: FG syndrome
FG syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nervous System Diseases Disease or Syndrome 19 12 0.010 None 1.000 1 1998 1998
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 61 7 0.010 None 1.000 1 2005 2005
CUI: C0011389
Disease: Dental Plaque
Dental Plaque
phenotype Stomatognathic Diseases Disease or Syndrome 27 0.010 None 1.000 1 2016 2016
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 2667 277 0.010 None 1.000 1 2009 2009
CUI: C0376338
Disease: Diagnosis, Psychiatric
Diagnosis, Psychiatric
disease Mental Disorders Mental or Behavioral Dysfunction 46 1 0.010 None 1.000 1 2016 2016
CUI: C4554601
Disease: Amyloidosis cutis dyschromia
Amyloidosis cutis dyschromia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 84 1 0.010 None 1.000 1 2017 2017
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.010 None 1.000 1 2019 2019
androgen independent prostate cancer
disease Neoplastic Process 190 5 0.010 None 1.000 1 2008 2008
CUI: C1275685
Disease: Avellino corneal dystrophy
Avellino corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 115 14 0.010 None 1.000 1 2017 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2020 2020
CUI: C0920652
Disease: skin irritant
skin irritant
phenotype Sign or Symptom 4 0.010 None 1.000 1 2001 2001
CUI: C0751097
Disease: Empty Sella Syndrome, Secondary
Empty Sella Syndrome, Secondary
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 1 0.300 None 1.000 1 2004 2004
CUI: C0750942
Disease: Auditory Inattention
Auditory Inattention
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 2 0.300 None 1.000 1 2004 2004
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6776 2793 0.010 None 1.000 1 2012 2012
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4388 1168 0.010 None 1.000 1 2008 2008
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder
disease Eye Diseases Disease or Syndrome 304 56 0.010 None 1.000 1 2017 2017
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
group Mental Disorders Mental or Behavioral Dysfunction 580 308 0.010 None 1.000 1 1993 1993
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.010 None 1.000 1 2008 2008
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 3720 652 0.010 None 1.000 1 2016 2016
CUI: C3495798
Disease: Periodontal inflammation
Periodontal inflammation
disease Disease or Syndrome 82 2 0.010 None 1.000 1 2018 2018
CUI: C0152427
Disease: Polydactyly
Polydactyly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 188 43 0.010 None 1.000 1 2003 2003
CUI: C0004310
Disease: Auditory Perceptual Disorders
Auditory Perceptual Disorders
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 5 0.300 None 1.000 1 2004 2004
CUI: C0024439
Disease: Macular corneal dystrophy
Macular corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 5 2 0.300 None 1.000 1 2002 2002
CUI: C0024205
Disease: Lymphadenitis
Lymphadenitis
disease Hemic and Lymphatic Diseases Disease or Syndrome 55 2 0.010 None 1.000 1 2018 2018