Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Characterizing rare and low-frequency height-associated variants in the Japanese population.
|
31562340 |
2019 |
Bone Density
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
|
19801982 |
2009 |
Bone Density
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
|
19801982 |
2009 |
Bone Density
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
New sequence variants associated with bone mineral density.
|
19079262 |
2009 |
Bone Density
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
|
22504420 |
2012 |
Bone Density
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
New sequence variants associated with bone mineral density.
|
19079262 |
2009 |
Bone Mineral Density Test
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Meta-analysis of gene-based genome-wide association studies of bone mineral density in Chinese and European subjects.
|
21927923 |
2012 |
Bone Mineral Density Test
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
|
22504420 |
2012 |
Osteogenesis Imperfecta
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Mutations of the Sp7 gene in humans are associated with craniofacial anomalies and osteogenesis imperfecta.
|
29405385 |
2018 |
Craniofacial Abnormalities
|
0.010 |
GeneticVariation
|
group |
BEFREE |
Mutations of the Sp7 gene in humans are associated with craniofacial anomalies and osteogenesis imperfecta.
|
29405385 |
2018 |
OSTEOGENESIS IMPERFECTA, TYPE XII
|
0.600 |
Biomarker
|
disease |
CTD_human |
|
|
|
OSTEOGENESIS IMPERFECTA, TYPE XII
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment.
|
29382611 |
2018 |
Dwarfism
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Micrognathism
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Microstomia
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Scoliosis, unspecified
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Congenital pectus carinatum
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Late tooth eruption
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Byzanthine arch palate
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Short stature
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Clumsiness - motor delay
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Facial asymmetry
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Depressed nasal bridge
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Prominent forehead
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Prominent supraorbital ridges
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|