GSN, gelsolin, 2934

N. diseases: 262; N. variants: 26
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 17 1999 2019
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis
disease Disease or Syndrome 2 1 0.020 None 1.000 2 1 1999 2019
CUI: C0221760
Disease: brain cyst
brain cyst
disease Disease or Syndrome 18 0.010 None 1.000 1 2011 2011
CUI: C0231818
Disease: Airway constriction
Airway constriction
phenotype Sign or Symptom 8 0.010 None 1.000 1 2019 2019
CUI: C0272138
Disease: Erythroblastosis
Erythroblastosis
disease Disease or Syndrome 89 0.010 None 1.000 1 1987 1987
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency
disease Disease or Syndrome 10 2 0.010 None 1.000 1 2017 2017
CUI: C0521175
Disease: Neuropil Threads
Neuropil Threads
disease Acquired Abnormality 13 0.010 None 1.000 1 2009 2009
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
disease Disease or Syndrome 297 3 0.010 None 1.000 1 2019 2019
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.010 None 1.000 1 1999 1999
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 1992 1992
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
disease Disease or Syndrome 10 1 0.010 None 1.000 1 2002 2002
Oestrogen receptor positive breast cancer
disease Neoplastic Process 510 58 0.010 None 1.000 1 2015 2015
CUI: C2939149
Disease: Amyloid of cornea
Amyloid of cornea
disease Disease or Syndrome 4 5 0.010 None 1.000 1 1 2014 2014
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
CUI: C3160889
Disease: Node-negative breast cancer
Node-negative breast cancer
disease Neoplastic Process 54 2 0.010 None 1.000 1 2015 2015
CUI: C1856507
Disease: Bulbar signs
Bulbar signs
phenotype Finding 33 1 0.100 None 0
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE
phenotype Finding 137 0.100 None 0
Distal peripheral sensory neuropathy
disease Disease or Syndrome 6 0.100 None 0
CUI: C4023402
Disease: Regional abnormality of skin
Regional abnormality of skin
disease Anatomical Abnormality 4 0.100 None 0
CUI: C4024863
Disease: Diffuse skin atrophy
Diffuse skin atrophy
disease Disease or Syndrome 3 0.100 None 0
Dermatological manifestations of systemic disorders
phenotype Finding 3 0.100 None 0
CUI: C4476761
Disease: Abnormal spleen morphology
Abnormal spleen morphology
phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C0011570
Disease: Mental Depression
Mental Depression
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1478 271 0.010 None < 0.001 1 2019 2019
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 332 56 0.010 None 1.000 1 2017 2017
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None < 0.001 1 2019 2019