Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C2931008
Disease: Congenital disorder of glycosylation type 2A
Congenital disorder of glycosylation type 2A 		0.920 CausalMutation CLINVAR

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0011998
Disease: Diastema of Teeth
Diastema of Teeth 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0024433
Disease: Macrostomia
Macrostomia 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0029453
Disease: Osteopenia
Osteopenia 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0152421
Disease: Macrotia
Macrotia 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0239137
Disease: Coxa valga
Coxa valga 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		0.100 Biomarker HPO

Entrez Id: 4247
Gene Symbol: MGAT2
MGAT2
CUI: C0241240
Disease: Tall stature
Tall stature 		0.100 Biomarker HPO