PODXL, podocalyxin like, 5420

N. diseases: 156; N. variants: 5
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: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.330 None 1.000 3 2006 2018
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
group Neoplasms; Male Urogenital Diseases Neoplastic Process 1722 31 0.320 None 1.000 2 2006 2018
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 31 9 0.310 strong 1.000 3 2014 2017
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 219 79 0.300 None 1.000 1 2011 2011
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 47 0.300 None 1.000 1 2011 2011
CUI: C0750986
Disease: Internal Carotid Artery Diseases
Internal Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2011 2011
CUI: C0040053
Disease: Thrombosis
Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 98 0.300 None 1.000 1 2011 2011
CUI: C0087086
Disease: Thrombus
Thrombus
phenotype Cardiovascular Diseases Pathologic Function 46 0.300 None 1.000 1 2011 2011
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 69 6 0.300 None 1.000 1 2011 2011
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 384 45 0.300 strong 1.000 1 2019 2019
CUI: C0750987
Disease: Arterial Diseases, Common Carotid
Arterial Diseases, Common Carotid
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2011 2011
CUI: C0600178
Disease: External Carotid Artery Diseases
External Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2011 2011
CUI: C4510873
Disease: Atypical juvenile parkinsonism
Atypical juvenile parkinsonism
disease Disease or Syndrome 4 0.300 None 1.000 1 2016 2016
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
disease Nervous System Diseases Disease or Syndrome 67 37 0.110 None 1.000 1 1 2016 2016
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.100 None 1.000 13 2007 2020
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 1 1 2019 2019
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Anatomical Abnormality 213 2 0.100 None 0
CUI: C0085632
Disease: Apathy
Apathy
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 83 9 0.100 None 0
CUI: C0085631
Disease: Agitation
Agitation
phenotype Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Sign or Symptom 109 4 0.100 None 0
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 126 72 0.100 None 0
CUI: C0040822
Disease: Tremor
Tremor
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 528 52 0.100 None 0
CUI: C0085623
Disease: Akinesia
Akinesia
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 43 3 0.100 None 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
disease Musculoskeletal Diseases Disease or Syndrome 850 135 0.100 None 0
CUI: C0036572
Disease: Seizures
Seizures
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2152 553 0.100 None 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
phenotype Finding 57 24 0.100 None 0