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: 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: C4023764
Disease: Elevated alkaline phosphatase of hepatic origin
Elevated alkaline phosphatase of hepatic origin 		phenotype Finding 3 0.100 None 0
CUI: C4022867
Disease: Spider hemangioma
Spider hemangioma 		disease Disease or Syndrome 4 0.100 None 0
CUI: C4020948
Disease: Palmar telangiectasia
Palmar telangiectasia 		disease Anatomical Abnormality 5 0.100 None 0
CUI: C4025612
Disease: Polyclonal elevation of IgM
Polyclonal elevation of IgM 		phenotype Finding 5 0.100 None 0
CUI: C4054912
Disease: Fusion-Positive Alveolar Rhabdomyosarcoma
Fusion-Positive Alveolar Rhabdomyosarcoma 		disease Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2018 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: C4551951
Disease: Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 8 9 0.010 None 1.000 1 2012 2012
CUI: C1562061
Disease: Microspherophakia
Microspherophakia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 9 0.010 None 1.000 1 2009 2009
CUI: C0341395
Disease: Perianal Crohn's disease
Perianal Crohn's disease 		disease Digestive System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 10 3 0.010 None 1.000 1 2016 2016
CUI: C0472762
Disease: Alpha trait thalassemia
Alpha trait thalassemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 3 0.010 None 1.000 1 2015 2015
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 13 4 0.010 None 1.000 1 2017 2017
CUI: C0333113
Disease: Sacculation
Sacculation 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Anatomical Abnormality 14 0.010 None 1.000 1 2015 2015
CUI: C4510788
Disease: Deep endometriosis
Deep endometriosis 		disease Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 14 0.010 None 1.000 1 2005 2005
CUI: C1274233
Disease: T-lymphocyte immunodeficiency
T-lymphocyte immunodeficiency 		disease Immune System Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2015 2015
CUI: C0009373
Disease: Colonic Diseases
Colonic Diseases 		group Digestive System Diseases Disease or Syndrome 17 8 0.010 None 1.000 1 2016 2016
CUI: C0344911
Disease: Left ventricular dilatation
Left ventricular dilatation 		disease Congenital Abnormality 17 3 0.010 None < 0.001 1 2017 2017
CUI: C0021832
Disease: Intestinal Diseases, Parasitic
Intestinal Diseases, Parasitic 		group Digestive System Diseases; Infections Disease or Syndrome 19 0.010 None 1.000 1 2015 2015
CUI: C0026265
Disease: Diseases of mitral valve
Diseases of mitral valve 		group Cardiovascular Diseases Disease or Syndrome 21 2 0.010 None 1.000 1 2009 2009
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 21 24 0.010 None 1.000 1 2019 2019
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection 		disease Infections Disease or Syndrome 21 1 0.010 None 1.000 1 2020 2020
CUI: C2936476
Disease: Chronic Liver Failure
Chronic Liver Failure 		disease Digestive System Diseases Disease or Syndrome 25 1 0.100 None 0
CUI: C0483368
Disease: Human anaplasmosis due to Anaplasma phagocytophilum
Human anaplasmosis due to Anaplasma phagocytophilum 		disease Infections; Animal Diseases Disease or Syndrome 29 0.010 None 1.000 1 1998 1998
CUI: C3826128
Disease: Infection in children
Infection in children 		disease Disease or Syndrome 29 5 0.010 None 1.000 1 2012 2012