SLC45A2, solute carrier family 45 member 2, 51151

N. diseases: 68; N. variants: 36
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: C1847836
Disease: Oculocutaneous Albinism, Type IV
Oculocutaneous Albinism, Type IV
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 3 21 0.950 1.000 16 21 1964 2017
CUI: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 2453 389 0.500 1.000 14 6 2002 2017
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
disease Neoplasms Neoplastic Process 1875 224 0.430 1.000 4 3 2002 2017
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
disease Neoplasms Neoplastic Process 106 56 0.400 2 1 2009 2016
CUI: C0001916
Disease: Albinism
Albinism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 50 16 0.330 1.000 4 1998 2016
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Congenital Abnormality 30 6 0.310 strong 1 2008 2008
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
disease Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 139 13 0.300 1 2010 2010
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
group Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 142 10 0.300 1 2010 2010
CUI: C0740858
Disease: Substance abuse problem
Substance abuse problem
disease Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 154 10 0.300 1 2010 2010
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders
group Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 122 2 0.300 1 2010 2010
CUI: C4316881
Disease: Prescription Drug Abuse
Prescription Drug Abuse
phenotype Mental Disorders; Substance-Related Disorders Finding 115 0.300 1 2010 2010
CUI: C1368275
Disease: Pigmented Basal Cell Carcinoma
Pigmented Basal Cell Carcinoma
disease Neoplasms Neoplastic Process 28 0.300 1 2009 2009
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
phenotype Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 174 18 0.300 1 2010 2010
Organic Mental Disorders, Substance-Induced
disease Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 115 0.300 1 2010 2010
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders
group Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 118 0.300 1 2010 2010
CUI: C0013170
Disease: Drug habituation
Drug habituation
phenotype Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 137 7 0.300 1 2010 2010
CUI: C0013146
Disease: Drug abuse
Drug abuse
disease Mental Disorders; Substance-Related Disorders Mental or Behavioral Dysfunction 228 25 0.300 1 2010 2010
CUI: C2673809
Disease: Infantile nystagmus
Infantile nystagmus
phenotype Finding 11 0.300 strong 0
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
disease Disease or Syndrome 5 13 0.200 1 1998 1998
CUI: C0268497
Disease: Brown oculocutaneous albinism
Brown oculocutaneous albinism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Congenital Abnormality 4 28 0.200 1 1998 1998
CUI: C0342683
Disease: ALBINISM, OCULOCUTANEOUS, TYPE III
ALBINISM, OCULOCUTANEOUS, TYPE III
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 4 3 0.200 1 1998 1998
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 6 46 0.200 1 1998 1998
CUI: C0268494
Disease: Oculocutaneous albinism type 1
Oculocutaneous albinism type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 9 87 0.200 1 1998 1998
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 3 18 0.200 1 1998 1998
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 3 9 0.200 1 1998 1998