Results: Osteochondrodysplasias

Results from Abstracts

Pick one of the followings

*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.

Legend:

***	p-value <= 0.001
**	p-value <= 0.01
*	p-value <= 0.05
n.s.	not significant

Top Ranked Genes, Molecules or Short Names*

Flnb *
Matn3 *
Col9a1 *
Col9a3 *
Col9a2 n.s.
Comp n.s.
Fgfr3 n.s.
Papss2 n.s.
Papss1 n.s.
Wdr34 n.s.
Dync2li1 n.s.
Wdr60 n.s.
Dync2h1 n.s.
Col27a1 n.s.
Chst3 n.s.
Fkbp10 n.s.
Ppib n.s.
Crtap n.s.
Serpinf1 n.s.
Plod2 n.s.
Slc26a2 n.s.
Tmem38b n.s.
Serpinh1 n.s.
Pls3 n.s.
Sp7 n.s.
Bmp1 n.s.
Col11a1 n.s.
Trpv4 n.s.
Col11a2 n.s.
Ihh n.s.
Flna n.s.
Col10a1 n.s.
Src n.s.
Sox9 n.s.
Wnt1 n.s.
Cyp11b1 n.s.
Gc n.s.
Col1a2 n.s.
Col2a1 n.s.
Ifitm5 n.s.
Sp1 n.s.
Tyr n.s.
Col1a1 n.s.
Rest n.s.
Mri n.s.
Cope n.s.
Large n.s.
Mb n.s.
Met n.s.
Set n.s.

Top Ranked Mesh Terms

Osteochondrodysplasias ***
Genetics ***
Child ***
Diagnostic imaging ***
Radiography ***
Humans ***
Male ***
Female ***
Infant newborn ***
Child preschool **
Pathology **
Adult **
Bone diseases developmental **
Diagnosis **
Infant **
Adolescent **
Pregnancy **
Mutation **
Cartilage **
Pedigree **
Phenotype **
Base sequence *
Ultrasonography prenatal *
Classification *
Dwarfism *
Collagen *
Prenatal diagnosis *
Osteogenesis imperfecta *
Point mutation *
Epidemiology *
Extracellular matrix *
Pregnancy complications *
Cervical vertebrae *
Arthritis *
Animals *
Thanatophoric dysplasia *
Genetic counseling *
Protein structure tertiary *
Skull *
Consanguinity *
Comparative genomic hybridization *
Hyaline membrane disease *
Abnormalities multiple *
Homozygote *
Chromosome disorders *
Face *
Achondroplasia *
Introns *
Bone and bones *
Fetal death *
Bronchial diseases *
Tracheal diseases *
Platybasia *
Down syndrome *
Codon *
Isoenzymes *
Thoracic vertebrae *
Lumbar vertebrae *
Orthopedics *
Genotype *
Parathyroid hormone-related protein *
Camurati-engelmann syndrome *
Sulfotransferases *
Chondrocytes *
Embryology *
Stillbirth *
Growth plate *
Dna primers *
Chromosome mapping *
Pregnancy outcome *
Femur *
Molecular sequence data *
Procollagen *
Collagen type ix *
Craniofacial abnormalities *
Diagnosis differential *
Abortion induced *
Amino acid substitution *
Joint instability *
Scoliosis *
Morphogenesis *
Proteoglycans *
Cross-sectional studies *
Intellectual disability *
Paternal age *
Sulfates *
Genes recessive *
Asphyxia neonatorum *
Protein processing post-translational *
Follow-up studies *
Fatal outcome *
Fetus *
Bone development *
Amino acid sequence *
Magnetic resonance imaging *
Cloning molecular *
Glycosaminoglycans *
Dna mutational analysis *
Cysteine *
Glycoproteins *

Results for: Osteochondrodysplasias

Results from Abstracts

KEGG Pathways

Gene Ontology Biological Processes