LRP1, LDL receptor related protein 1, 4035

N. diseases: 252; N. variants: 23
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: C0263428
Disease: Burnett Schwartz Berberian syndrome
Burnett Schwartz Berberian syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 5 1 0.520 None 1.000 2 1 2015 2018
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
group Nervous System Diseases Disease or Syndrome 512 264 0.480 None 1.000 11 1 2011 2018
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.420 None 1.000 4 4 2015 2019
CUI: C0338480
Disease: Common Migraine
Common Migraine
disease Nervous System Diseases Disease or Syndrome 77 62 0.400 None 1.000 3 1 2012 2016
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2872 2897 0.310 None 1.000 2 2011 2019
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 1236 1451 0.310 None 1.000 1 2010 2010
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
disease Mental Disorders Mental or Behavioral Dysfunction 641 225 0.310 None 1.000 1 2010 2010
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.300 None 0.935 46 2 1996 2019
CUI: C0007852
Disease: Cervical Migraine Syndrome
Cervical Migraine Syndrome
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0263429
Disease: Atrophoderma vermiculatum
Atrophoderma vermiculatum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.300 None 1.000 1 2015 2015
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0338489
Disease: Status Migrainosus
Status Migrainosus
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0343057
Disease: Keratosis pilaris decalvans
Keratosis pilaris decalvans
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 3 0.300 None 1.000 1 2015 2015
CUI: C0700438
Disease: Sick Headaches
Sick Headaches
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0521664
Disease: Acute Confusional Migraine
Acute Confusional Migraine
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0018984
Disease: Hemicrania migraine
Hemicrania migraine
disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2011 2011
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 2803 824 0.210 None 1.000 2 2012 2017
CUI: C0035320
Disease: Retinal Neovascularization
Retinal Neovascularization
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Pathologic Function 12 0.200 None 1.000 1 2006 2006
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy
disease Nervous System Diseases Disease or Syndrome 115 0.200 None 1.000 1 2016 2016
CUI: C0154088
Disease: Carcinoma in situ of prostate
Carcinoma in situ of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 6 0.200 None 1.000 1 2003 2003
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 235 0.200 None 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 85 13 0.200 None 0
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
group Cardiovascular Diseases Disease or Syndrome 108 1 0.200 None 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 925 294 0.200 None 0
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia
phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 78 3 0.200 None 0