Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.420 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
Sensorineural Hearing Loss (disorder)
0.410 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.150 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome
0.110 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0003862
Disease: Arthralgia
Arthralgia
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0024003
Disease: Lordosis
Lordosis
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0025995
Disease: Micromelia
Micromelia
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0026034
Disease: Microstomia
Microstomia
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0027092
Disease: Myopia
Myopia
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0038379
Disease: Strabismus
Strabismus
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
Hearing Loss, Mixed Conductive-Sensorineural
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0162298
Disease: Joint stiffness
Joint stiffness
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
0.100 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0239234
Disease: Low set ears
Low set ears
0.100 Biomarker HPO