GLMN, glomulin, FKBP associated protein, 11146

N. diseases: 28; N. variants: 9
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: C1841984
Disease: GLOMUVENOUS MALFORMATIONS
GLOMUVENOUS MALFORMATIONS
disease Neoplasms Disease or Syndrome 13 3 0.800 None 0.917 12 3 2002 2019
CUI: C0265950
Disease: Venous malformation
Venous malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 38 3 0.120 None 1.000 2 1999 2002
CUI: C2937220
Disease: Congenital abnormality of vein
Congenital abnormality of vein
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 39 7 0.120 None 1.000 2 2 1999 2002
CUI: C0346072
Disease: Blue rubber bleb nevus syndrome
Blue rubber bleb nevus syndrome
disease Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases Congenital Abnormality 3 1 0.110 None 1.000 1 1 2019 2019
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
phenotype Laboratory or Test Result 139 296 0.100 None 1.000 1 2 2016 2016
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
phenotype Laboratory Procedure 139 296 0.100 None 1.000 1 2 2016 2016
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
phenotype Laboratory Procedure 610 1144 0.100 None 1.000 1 1 2019 2019
CUI: C4020900
Disease: Abnormality of the upper limb
Abnormality of the upper limb
phenotype Anatomical Abnormality 6 4 0.100 None 0
CUI: C4021157
Disease: Generalized abnormality of skin
Generalized abnormality of skin
disease Anatomical Abnormality 3 1 0.100 None 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology
disease Congenital Abnormality 35 3 0.100 None 0
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum
phenotype Anatomical Abnormality 12 0.100 None 0
CUI: C4023763
Disease: Abnormality of the nasal cavity
Abnormality of the nasal cavity
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C4025678
Disease: Abnormal trachea morphology
Abnormal trachea morphology
phenotype Anatomical Abnormality 2 1 0.100 None 0
CUI: C4531113
Disease: Oral mucosa nodule
Oral mucosa nodule
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C1519353
Disease: Skin Papule
Skin Papule
phenotype Skin and Connective Tissue Diseases Finding 74 0.100 None 0
CUI: C0241148
Disease: Cutaneous plaque
Cutaneous plaque
phenotype Finding 19 107 0.100 None 0
CUI: C1096086
Disease: Deformity of lower limb
Deformity of lower limb
disease Anatomical Abnormality 11 5 0.100 None 0
Gastrointestinal arteriovenous malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 3 0.100 None 0
CUI: C0332563
Disease: Papule
Papule
phenotype Pathological Conditions, Signs and Symptoms Finding 76 131 0.100 None 0
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 106 16 0.100 None 0
CUI: C0037287
Disease: Skin nodule
Skin nodule
disease Neoplasms; Skin and Connective Tissue Diseases Pathologic Function 8 0.100 None 0
CUI: C0334421
Disease: Glomangioma
Glomangioma
disease Neoplasms Neoplastic Process 1 0.020 None 1.000 2 2002 2005
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 1740 865 0.010 None 1.000 1 2006 2006
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1043 127 0.010 None 1.000 1 2019 2019