LAMC2, laminin subunit gamma 2, 3918

N. diseases: 602; N. variants: 66
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: C1955760
Disease: Idiopathic normal pressure hydrocephalus (INPH)
Idiopathic normal pressure hydrocephalus (INPH) 		disease Disease or Syndrome 25 0.100 None 1.000 16 2017 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.100 None 1.000 15 2013 2019
CUI: C1141920
Disease: Shunt infection
Shunt infection 		disease Disease or Syndrome 5 0.050 None 1.000 5 2017 2019
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
PARKINSON DISEASE, LATE-ONSET 		disease Disease or Syndrome 247 76 0.050 None 1.000 5 2018 2020
CUI: C1455718
Disease: Neurological ventriculitis
Neurological ventriculitis 		disease Disease or Syndrome 10 0.040 None 1.000 4 2017 2019
CUI: C2921627
Disease: Clinically isolated syndrome
Clinically isolated syndrome 		disease Disease or Syndrome 54 2 0.040 None 1.000 4 2019 2019
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		disease Neoplastic Process 860 154 0.030 None 1.000 3 2017 2019
CUI: C1095979
Disease: Progressive multiple sclerosis
Progressive multiple sclerosis 		disease Disease or Syndrome 37 0.030 None 1.000 3 2017 2019
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease Disease or Syndrome 271 13 0.030 None 1.000 3 2017 2019
CUI: C0039147
Disease: Syrinx formation
Syrinx formation 		disease Anatomical Abnormality 18 0.020 None 1.000 2 2017 2019
CUI: C0393446
Disease: Bacterial ventriculitis
Bacterial ventriculitis 		disease Disease or Syndrome 4 0.020 None 1.000 2 2017 2019
CUI: C0848633
Disease: Sinus pressure
Sinus pressure 		phenotype Sign or Symptom 2 0.020 None 1.000 2 2017 2019
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.020 None 1.000 2 2017 2019
CUI: C3805043
Disease: Vascular cognitive impairment
Vascular cognitive impairment 		disease Disease or Syndrome 42 1 0.020 None 1.000 2 2018 2019
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		disease Disease or Syndrome 985 56 0.020 None 1.000 2 2018 2019
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		disease Disease or Syndrome 12 8 0.020 None 0.500 2 2018 2019
CUI: C4285807
Disease: Behavioral and psychological symptoms of dementia
Behavioral and psychological symptoms of dementia 		phenotype Sign or Symptom 72 9 0.020 None 1.000 2 2017 2019
CUI: C0009812
Disease: Constitutional Symptom
Constitutional Symptom 		phenotype Sign or Symptom 30 1 0.010 None 1.000 1 2017 2017
CUI: C0015826
Disease: Fenestration (morphologic abnormality)
Fenestration (morphologic abnormality) 		disease Acquired Abnormality 43 0.010 None 1.000 1 2017 2017
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		group Disease or Syndrome 188 9 0.010 None 1.000 1 2019 2019
CUI: C0233401
Disease: Psychiatric symptom
Psychiatric symptom 		phenotype Sign or Symptom 95 12 0.010 None < 0.001 1 2019 2019
CUI: C0338474
Disease: Central nervous system demyelination
Central nervous system demyelination 		disease Disease or Syndrome 52 3 0.010 None 1.000 1 2018 2018
CUI: C0339821
Disease: Concha bullosa
Concha bullosa 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0340766
Disease: Venous hypertension
Venous hypertension 		disease Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0426980
Disease: Motor symptoms
Motor symptoms 		phenotype Sign or Symptom 100 15 0.010 None 1.000 1 2018 2018