Results: Achondroplasia

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*

Fgfr3 ***
Cnp *
Col11a2 *
Idua *
Msx2 *
Col11a1 *
Ptn *
Trappc2 *
Ado *
She *
Fgfr2 *
Col2a1 *
Comp *
Frs2 *
Jak1 n.s.
Fgf9 n.s.
Fgf2 n.s.
Pgd n.s.
Fgf1 n.s.
Cast n.s.
Cbl n.s.
Stat1 n.s.
Tk1 n.s.
Ihh n.s.
Hras n.s.
Fgfr1 n.s.
Fgf21 n.s.
Nppc n.s.
Tyr n.s.
Pth n.s.
Mri n.s.
Shox n.s.
Bad n.s.
Col9a2 n.s.
Col9a3 n.s.
Pmp22 n.s.
Sox6 n.s.
Sox5 n.s.
Fgf23 n.s.
Son n.s.
Chat n.s.
Acvr1 n.s.
Rnf11 n.s.
Acan n.s.
Gon4l n.s.
Sry n.s.
B4galt7 n.s.
Prkg2 n.s.
Spry2 n.s.
Tpo n.s.
Pthlh n.s.
Fibp n.s.
Sox9 n.s.
Rhd n.s.
Bmp4 n.s.
Evc n.s.
Evc2 n.s.
Matn3 n.s.
Smarcal1 n.s.
Trps1 n.s.
Phex n.s.
Arse n.s.
Npr2 n.s.
Rd3 n.s.
Twist1 n.s.
Fgfrl1 n.s.
Fgf7 n.s.
Fgf22 n.s.
Cdk2 n.s.
Ift20 n.s.
Flt4 n.s.
Ung n.s.
Stat5b n.s.
Atg12 n.s.
Fgf18 n.s.
Edaradd n.s.
C5 n.s.
Grb10 n.s.
Fgf8 n.s.
Gjb2 n.s.
Gh1 n.s.
Mcc n.s.
Slc13a1 n.s.
Ankh n.s.
Cdc37 n.s.
Magea4 n.s.
Enpp1 n.s.
Lpa n.s.
Sp3 n.s.
Fyn n.s.
Ptpn11 n.s.
Smurf1 n.s.
Stat5a n.s.
Fgf6 n.s.
Pvr n.s.
Col10a1 n.s.
Jak3 n.s.
Ighd n.s.
Atg5 n.s.
Nf1 n.s.

Top Ranked Key Phrases

C type natriuretic peptide cnp ***
Ellis van creveld syndrome ***
Fibroblast growth factor receptor 3 ***
Osteogenesis imperfecta type ii ***
Sleep disordered breathing ***
Obstructive sleep apnea ***
Increased intracranial pressure ***
Idiopathic short stature ***
Upper airway obstruction ***
Endochondral bone growth ***
Wild type mice ***
Disproportionate short stature ***
Short limbed dwarfism ***
Foramen magnum stenosis ***
Thanatophoric dysplasia td ***
Fgfr3 ach mice **
Common genetic form **
Growth hormone *
Wild type *
Spinal cord *
Spinal canal *
Growth plate *
Foramen magnum *
Growth plates *
Bone growth *
Tibial lengthening *
Short stature *
Cord compression *
Limb lengthening *
Spinal stenosis *
Bone formation *
Growth velocity *
Bone dysplasias *
Gh therapy n.s.
Head circumference n.s.
Skeletal dysplasias n.s.
Osteogenesis imperfecta n.s.
Femoral lengthening n.s.
Humeral lengthening n.s.
Skeletal dysplasia n.s.
Fgf signaling n.s.
Achondroplastic dwarf n.s.
Mutant fgfr3 n.s.
Cervicomedullary junction n.s.
Cranial base n.s.
Chondrocyte proliferation n.s.
Common type n.s.
Fgfr3 signaling n.s.
Cervicomedullary compression n.s.
Maternal plasma n.s.
Congenital anomalies n.s.
Growth rate n.s.
Ligamentum flavum n.s.
Thoracolumbar kyphosis n.s.
Lumbar lordosis n.s.
Study was n.s.
Long bones n.s.
Thanatophoric dysplasia n.s.
Developmental delay n.s.
Genetic disorders n.s.
Molecular analysis n.s.
Sitting height n.s.
G380r mutation n.s.
Lumbar spine n.s.
Genetic counseling n.s.
Sudden death n.s.
Endochondral ossification n.s.
Point mutation n.s.
G1138a mutation n.s.
Mouse model n.s.
S syndrome n.s.
Distraction osteogenesis n.s.
Large head n.s.
Transmembrane domain n.s.
Final height n.s.
Human dwarfism n.s.
Diastrophic dysplasia n.s.
Gh treatment n.s.
S disease n.s.
Fgfr3 gene n.s.
Neurogenic claudication n.s.

Top Ranked Mesh Terms

Postoperative complications ***
Middle aged ***
Diagnostic imaging ***
Diagnosis ***
Cervical vertebrae ***
Signal transduction ***
Bone diseases developmental ***
Chondrocytes ***
Thanatophoric dysplasia ***
Femur ***
Adolescent ***
Heterozygote ***
Spine ***
Genetics ***
Bone development ***
Protein-tyrosine kinases ***
Infant ***
Diagnosis differential ***
Point mutation ***
Receptor fibroblast growth factor type 3 ***
Pedigree ***
Tibia ***
Dwarfism ***
Prenatal diagnosis ***
Bone lengthening ***
Mutation ***
Animals ***
Pregnancy ***
Female ***
Radiography ***
Metabolism ***
Child ***
Phenotype ***
Epidemiology ***
Spinal cord compression ***
Skull ***
Body height ***
Retrospective studies ***
Bone and bones ***
Cartilage ***
Mice ***
Young adult ***
Achondroplasia ***
Lumbar vertebrae ***
Growth plate ***
Male ***
Magnetic resonance imaging ***
Treatment outcome ***
Adult ***
Physiology ***
Osteochondrodysplasias ***
Methods ***
Child preschool ***
Age factors ***
Decompression surgical ***
Foramen magnum ***
Cell differentiation ***
Humans ***
Receptors fibroblast growth factor ***
Infant newborn ***
Ultrasonography prenatal ***
Pathology ***
Tomography x-ray computed ***
Follow-up studies ***
Base sequence ***
Mice transgenic ***
Laminectomy ***
Amino acid substitution ***
Growth disorders ***
Polymerase chain reaction ***
Sleep apnea syndromes ***
Osteogenesis imperfecta ***
Lordosis ***
Aged ***
Spinal stenosis ***
Disease models animal ***
Hydrocephalus ***
Dna mutational analysis **
Kyphosis **
Phosphorylation **
Drug therapy **
Dna **
Natriuretic peptide c-type **
Paternal age **
Syndrome **
Molecular sequence data **
Thoracic vertebrae **
Limb deformities congenital **
Growth and development **
Amino acid sequence **
Fetal diseases **
Osteogenesis **
Mutation missense **
Cohort studies **
Risk factors **
Osteotomy **
Craniosynostoses **
Constriction pathologic **
Fibroblast growth factors **
Homozygote **

Top Ranked Mesh Terms (Symptoms)

Postoperative complications ***
Growth disorders ***
Syndrome **
Constriction pathologic **
Chromosome aberrations **
Intellectual disability *
Body weight *
Hypoxia *
Obesity morbid *
Death sudden *
Blindness *
Leg length inequality *
Atrophy *
Urinary bladder neurogenic *
Paresthesia *
Sleep wake disorders *
Chromosome deletion *
Dyspnea *
Psychomotor disorders *
Vision disorders *
Hearing loss conductive *
Intraoperative complications *
Hearing loss *
Rare diseases *
Birth weight *
Genetic predisposition to disease n.s.
Paraplegia n.s.
Ossification heterotopic n.s.
Cell transformation neoplastic n.s.
Hypertrophy n.s.
Obesity n.s.
Apnea n.s.
Facies n.s.
Pain n.s.
Fetal death n.s.
Hearing loss sensorineural n.s.
Seizures n.s.
Recurrence n.s.
Snoring n.s.
Headache n.s.
Pain postoperative n.s.
Aneuploidy n.s.
Sudden infant death n.s.
Disease progression n.s.
Fetal growth retardation n.s.
Chronic disease n.s.
Quadriplegia n.s.
Diseases in twins n.s.
Muscle hypotonia n.s.
Low back pain n.s.
Intermittent claudication n.s.
Chronic pain n.s.
Hematoma epidural cranial n.s.
Deafness n.s.
Mobility limitation n.s.
Trisomy n.s.
Nausea n.s.
Vomiting n.s.
Amenorrhea n.s.
Weight loss n.s.
Hemifacial spasm n.s.
Osteonecrosis n.s.
Hypoventilation n.s.
Learning disorders n.s.
Hernia inguinal n.s.
Hearing disorders n.s.
Reflex abnormal n.s.
Back pain n.s.
Translocation genetic n.s.
Cadaver n.s.
Cysts n.s.
Perinatal death n.s.
Nondisjunction genetic n.s.
Choristoma n.s.
Arthralgia n.s.
Kidney calculi n.s.
Confusion n.s.
Mouth breathing n.s.
Intracranial hemorrhages n.s.
Hematoma n.s.
Encephalocele n.s.
Sex chromosome aberrations n.s.
Hernia n.s.
Olfaction disorders n.s.
Menstruation disturbances n.s.
Cerebral hemorrhage n.s.
Facial paralysis n.s.
Pelvic organ prolapse n.s.
Polyps n.s.
Abdominal pain n.s.
Cafe-au-lait spots n.s.
Paralysis n.s.
Intervertebral disc displacement n.s.
Sclerosis n.s.
Hyperplasia n.s.
Arteriovenous fistula n.s.
Prosthesis failure n.s.
Surgical wound infection n.s.
Surgical wound dehiscence n.s.
Cerebrospinal fluid leak n.s.

Results for: Achondroplasia

Results from Abstracts

KEGG Pathways

Gene Ontology Biological Processes