achondroplasia (Also achondroplasias) : Related Words Words similar in meaning to achondroplasia
- osteosclerosis congenita«
- chondrodystrophy«
- achondroplasty«
- achondroplasia«
- rhizomelia«
- dwarfism«
- achondroplastic«
- congenital disease«
- hypochondroplasia«
- mutant gene«
- genetic«
- disproportionate dwarfism«
- genetic abnormality«
- mutation«
- inherited disorder«
- disorder«
- thanatophoric dysplasia«
- genetic disorder«
- hydrocephalus«
- genetic defect«
- achondroplasic«
- diagnosis«
- inherited disease«
- piglet«
- hereditary disease«
- hereditary condition«
- human«
- genetic disease«
- birth«
- trident hand configuration«
- trident hand«
- trident configuration«
- thoracolumbar gibbus«
- small midface«
- radiologic findings«
- prominent forehead frontal«
- progressive discordance«
- prevalence difficult«
- normal development fgfr3«
- normal danish sow«
- new gene mutation«
- narrowed spinal canal«
- narrow sciatic notch«
- narrow foramen magnum«
- multiple epiphyseal dysplasia tarda«
- mild skeletal disorder«
- limbed dog«
- irregular growth plate«
- intervertebral disk height«
- horizontal acetabular roof«
- homozygous child«
- genetic basis similar«
- g595e«
- fibular overgrowth«
- extinct ancon sheep«
- deformed bone structure«
- controversial surgery«
- common domestic sheep«
- beneficial bone growth«
- annualized growth velocity«
- altered cell pattern«
- achondroplastic adult«
- litter«
- subjective diagnostic criterion«
- spinal kyphosis«
- sized torso«
- schmid metaphyseal chondrodysplasia«
- rhizomelic shortening«
- metaphyseal cupping«
- col10a1 gene«
- achondroplastic dog breed«
- vosoritide«
- negative regulatory effect«
- flattened nasal bridge«
- facial hypoplasia«
- eustachian tube blockage«
- syndrome«
- gh therapy«
- genome association study«
- future treatment option«
- biomarin pharmaceutical inc.«
- study«
- prevalence«
- short metacarpal«
- iliac wing«
- fgfr3 gene«
- biparietal diameter«
- average adult height«
- skeletal survey«
- affected sheep«
- advanced paternal age«
- proximal limb«
- mutant copy«
- growth hormone therapy«
- infancy«
- concave curvature«
- lethal allele«
- dental malocclusion«
- achondrogenesis«
- therapy«
- protein collagen«
- fetal ultrasound«
- tubular bone«
- large head«
- convex curvature«
- offspring«
- sporadic mutation«
- radiographic feature«
- biomarin«
- lethal condition«
- autosomal dominant genetic disorder«
- type natriuretic peptide«
- similar mutation«
- upper airway obstruction«
- prenatal ultrasound«
- femur length«
- short finger«
- valgus«
- parent«
- fibroblast growth factor receptor«
- bowleg«
- osteopetrosis«
- prominent forehead«
- similar presentation«
- histological study«
- type x«
- lordosis«
- growth factor receptor«
- skull base«
- radiographic finding«
- gene coding«
- homozygosity«
- flaring«
- spontaneous mutation«
- oogenesis«
- kyphosis«
- vertebral body«
- short limb«
- varus«
- congenital condition«
- osteogenesis imperfecta«
- otitis medium«
- healthy volunteer«
- basset hound«
- fibroblast growth factor«
- bone growth«
- regulatory mechanism«
- gene mutation«
- spermatogenesis«
- distinct characteristic«
- human growth hormone«
- dachshund«
- sleep apnea«
- ear infection«
- corgi«
- term treatment«
- stillbirth«
- dog breed«
- clinical feature«
- leg«
- people«
- other animal«
- similar form«
- short stature«
- selective breeding«
- strong association«
- phalanx«
- shortening«
- % chance«
- deformity«
- dna test«
- cutaneous condition«
- copy«
- cartilage«
- female«
- positive result«
- live birth«
- retro«
- spinal cord«
- causes«
- child«
- treatment«
- compression«
- receptor«
- bulldog«
- analog«
- wool«
- rib«
- maturity«
- alpha«
- limb«
- toe«
- likelihood«
- trait«
- cure«
- skull«
- father«
- complication«
- gene«
- sheep«
- knee«
- meat«
- finger«
- estimate«
- age«
- bone«
- dog«
- ichthyosis«
- otosclerosis«
- polygenic disorder«
- polygenic disease«
- congenital megacolon«
- porphyria«
- nevoid elephantiasis«
- congenital pancytopenia«
- congenital afibrinogenemia«
- monogenic disorder«
- monogenic disease«
- autosomal recessive disease«
- autosomal recessive defect«
- autosomal dominant disorder«
- autosomal dominant disease«
- lactase deficiency«
- lactose intolerance«
- muscular dystrophy«
- dystrophy«
- inborn error of metabolism«
- hepatolenticular degeneration«
- juvenile amaurotic idiocy«
- branched chain ketoaciduria«
- maple syrup urine disease«
- marble bones disease«
- milk intolerance«
- pachyderma«
- oligodontia«
- oligodactyly«
- nanism«
- mucopolysaccharidosis«
- hyperbetalipoproteinemia«
- abetalipoproteinemia«
- myotonic muscular dystrophy«
- myotonic dystrophy«
- phenylketonuria«
- xeroderma«
- myotonia atrophica«
- sickle-cell disease«
- sickle-cell anemia«
- sickle-cell anaemia«
- thalassaemia«
- familial hypercholesterolemia«
- galactosemia«
- thalassemia«
- fibrocystic disease of the pancreas«
- drepanocytic anaemia«
- crescent-cell anaemia«
- neurofibromatosis«
- cystic fibrosis«
- severe combined immunodeficiency disease«
- severe combined immunodeficiency«
- pancreatic fibrosis«
- drepanocytic anemia«
- crescent-cell anemia«
- infantile amaurotic idiocy«
- pseudohypertrophic dystrophy«
- oculopharyngeal muscular dystrophy«
- limb-girdle muscular dystrophy«
- distal muscular dystrophy«
- malignant hyperthermia«
- diabetes«
- von Recklinghausen's disease«
- dysostosis multiplex«
- xerodermia«
- tyrosinemia«
- thrombasthenia«
- pycnodysostosis«
- mucoviscidosis«
- lysinemia«
- lipochondrodystrophy«
- gargoylism«
- Fanconi's anaemia«
- Fanconi's anemia«
- Wilson's disease«
- Spielmeyer-Vogt disease«
- McArdle's disease«
- Hirschsprung's disease«
- Albers-Schonberg disease«
- Mediterranean anaemia«
- Mediterranean anemia«
- Huntington's chorea«
- Marfan's syndrome«
- Hurler's syndrome«
- Duchenne's muscular dystrophy«
- Becker muscular dystrophy«
- Werdnig-Hoffman disease«
- Tay-Sachs disease«
- Steinert's disease«
- Sachs disease«
- Niemann-Pick disease«
- Hurler's disease«
- Huntington's disease«
- Gaucher's disease«
- Tay-Sachs«
- SCID«
- PKU«