POGLUT1, protein O-glucosyltransferase 1, 56983

N. diseases: 36; N. variants: 8
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.
Proximal muscle weakness in lower limbs
phenotype Finding 30 4 0.100 None 0
CUI: C0240953
Disease: Winged scapula
Winged scapula
phenotype Finding 73 3 0.100 None 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis
phenotype Finding 16 0.100 None 0
CUI: C0221270
Disease: Acanthosis
Acanthosis
phenotype Pathological Conditions, Signs and Symptoms Finding 37 0.100 None 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
phenotype Respiratory Tract Diseases Pathologic Function 315 15 0.100 None 0
Creatine phosphokinase serum increased
phenotype Finding 228 43 0.100 None 0
Reticulate acropigmentation of Kitamura
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 5 5 0.300 None 0
CUI: C4552092
Disease: Dowling-Degos disease 1
Dowling-Degos disease 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 4 3 0.300 None 0
CUI: C3810313
Disease: DOWLING-DEGOS DISEASE 4
DOWLING-DEGOS DISEASE 4
disease Disease or Syndrome 1 6 0.600 strong 1.000 2 6 2014 2017
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 21
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 1 1 0.600 moderate 1.000 2 1 2016 2017
CUI: C3714534
Disease: dowling-degos disease
dowling-degos disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 53 7 0.620 strong 1.000 3 2014 2017