MST1, macrophage stimulating 1, 4485

N. diseases: 281; N. variants: 4
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 0.938 16 2005 2019
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.040 None 1.000 4 2007 2018
CUI: C3553943
Disease: T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS 		disease Disease or Syndrome 8 1 0.030 None 0.667 3 2016 2019
CUI: C0220613
Disease: Adult Soft Tissue Sarcoma
Adult Soft Tissue Sarcoma 		disease Neoplastic Process 162 3 0.010 None 1.000 1 2007 2007
CUI: C0220645
Disease: Childhood Soft Tissue Sarcoma
Childhood Soft Tissue Sarcoma 		disease Neoplastic Process 166 3 0.010 None 1.000 1 2007 2007
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV 		disease Neoplastic Process 573 14 0.010 None 1.000 1 2012 2012
CUI: C0344911
Disease: Left ventricular dilatation
Left ventricular dilatation 		disease Congenital Abnormality 17 3 0.010 None < 0.001 1 2017 2017
CUI: C0857175
Disease: Postinfarction
Postinfarction 		disease Disease or Syndrome 49 1 0.010 None < 0.001 1 2017 2017
CUI: C1378050
Disease: Oncocytic Neoplasm
Oncocytic Neoplasm 		disease Neoplastic Process 105 2 0.010 None 1.000 1 2003 2003
CUI: C1840264
Disease: IMMUNE SUPPRESSION
IMMUNE SUPPRESSION 		phenotype Disease or Syndrome 222 3 0.010 None 1.000 1 2013 2013
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 3 2018 2018
CUI: C3826128
Disease: Infection in children
Infection in children 		disease Disease or Syndrome 29 5 0.010 None 1.000 1 2012 2012
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 0.010 None 1.000 1 2016 2016
CUI: C3898127
Disease: Non-Metastatic Childhood Soft Tissue Sarcoma
Non-Metastatic Childhood Soft Tissue Sarcoma 		disease Neoplastic Process 160 3 0.010 None 1.000 1 2007 2007
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		disease Anatomical Abnormality 83 20 0.010 None 1.000 1 2019 2019
CUI: C4732730
Disease: Blood spots
Blood spots 		disease Disease or Syndrome 117 0.010 None 1.000 1 2011 2011
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		phenotype Pathologic Function 70 0.100 None 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		disease Disease or Syndrome 56 6 0.100 None 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype Finding 212 9 0.100 None 0
CUI: C4020948
Disease: Palmar telangiectasia
Palmar telangiectasia 		disease Anatomical Abnormality 5 0.100 None 0
CUI: C4021050
Disease: Dilated superficial abdominal veins
Dilated superficial abdominal veins 		phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C4022766
Disease: Abnormal large intestine physiology
Abnormal large intestine physiology 		phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C4022867
Disease: Spider hemangioma
Spider hemangioma 		disease Disease or Syndrome 4 0.100 None 0
CUI: C4023764
Disease: Elevated alkaline phosphatase of hepatic origin
Elevated alkaline phosphatase of hepatic origin 		phenotype Finding 3 0.100 None 0
CUI: C4025612
Disease: Polyclonal elevation of IgM
Polyclonal elevation of IgM 		phenotype Finding 5 0.100 None 0