chondrodystrophy : Related Words Words similar in meaning to chondrodystrophy
- achondroplasia«
- osteosclerosis congenita«
- achondroplasty«
- chondrodystrophy«
- achondroplastic«
- inherited disorder«
- offspring«
- parent«
- inherited disease«
- allele«
- hereditary disease«
- child«
- hereditary condition«
- normal stature«
- genetic disorder«
- % chance«
- genetic disease«
- short limb«
- genetic defect«
- probability«
- genetic abnormality«
- t allele«
- congenital disease«
- little people«
- dwarf athletic association«
- disorder«
- carrier«
- skeletal dysplasia«
- recessive allele«
- diagnosis«
- dwarfism«
- copy«
- bone«
- extremity«
- trunk dysplasia«
- switch extenders«
- statured child«
- stature offspring«
- standard mendelian punnett square«
- short limb dysplasia«
- recessive allele coding«
- reabsorb«
- ranch fence«
- parent testing«
- other probability«
- normal size extremity«
- myriad genetic mutation«
- most common therapy«
- most childhood limb growth«
- modification suggestions«
- life/treatment«
- individual experience independence«
- genetic hyaline disorder«
- chondrodystrophy patient«
- chondrodystrophy gene«
- chondrodystrophic trait«
- chondrodystrophic offspring«
- cartilage maldevelopment«
- ancon_(sheep«
- fetus«
- specific skeletal dysplasia«
- percentage risk«
- effective driving«
- defective cartilage«
- cartilage form«
- statured person«
- smooth joint«
- hormonal injection«
- bone growth pattern«
- autosomal allele«
- joint margin«
- sized trunk«
- joint«
- body result«
- average parent«
- modified equipment«
- allele combination«
- chondrodysplasia«
- trunk«
- mendelian ratio«
- joint cartilage«
- inheritance«
- spinal vertebra«
- hormonal disorder«
- genu varum«
- jump«
- ball handling«
- autosomal«
- skeletal disorder«
- volleyball net«
- height adjustment«
- power lifting«
- hyaline cartilage«
- normal wear«
- surgical center«
- interior portion«
- dominant allele«
- swimming«
- common sport«
- orthopedist«
- racquet sport«
- ray«
- normal height«
- substantial effect«
- roam«
- precise description«
- bone growth«
- type«
- athlete«
- affected individual«
- random selection«
- apnea«
- autosomal recessive disorder«
- several organization«
- athletic performance«
- endocrinologist«
- bicycling«
- internist«
- adult patient«
- racquet«
- scoliosis«
- lethal dose«
- disease«
- risk«
- motor skill«
- growth hormone«
- normal size«
- family physician«
- growth«
- leg«
- osteoarthritis«
- presentation«
- metabolic«
- certain type«
- genetic testing«
- international paralympic committee«
- medical literature«
- animal«
- research purpose«
- america«
- national event«
- track event«
- neurologist«
- cartilage«
- phenotype«
- geneticist«
- arthritis«
- paralympic game«
- eyesight«
- pediatrics«
- pedal«
- causes«
- mating«
- appliance«
- obesity«
- sports«
- annual conference«
- common form«
- treatment«
- dwarf«
- chromosome«
- stature«
- mother«
- people«
- bowling«
- lamb«
- physical education«
- shaft«
- swing«
- playground«
- disadvantage«
- onset«
- father«
- ratio«
- gene«
- volleyball«
- tear«
- outcome«
- procedure«
- porphyria«
- polygenic disorder«
- polygenic disease«
- pachyderma«
- otosclerosis«
- osteopetrosis«
- oligodontia«
- oligodactyly«
- nevoid elephantiasis«
- nanism«
- muscular dystrophy«
- mucopolysaccharidosis«
- monogenic disorder«
- monogenic disease«
- milk intolerance«
- marble bones disease«
- maple syrup urine disease«
- lactose intolerance«
- lactase deficiency«
- juvenile amaurotic idiocy«
- inborn error of metabolism«
- ichthyosis«
- hyperbetalipoproteinemia«
- hepatolenticular degeneration«
- dystrophy«
- congenital pancytopenia«
- congenital megacolon«
- congenital afibrinogenemia«
- branched chain ketoaciduria«
- autosomal recessive disease«
- autosomal recessive defect«
- autosomal dominant disorder«
- autosomal dominant disease«
- abetalipoproteinemia«
- xerodermia«
- xeroderma«
- von Recklinghausen's disease«
- tyrosinemia«
- thrombasthenia«
- thalassemia«
- thalassaemia«
- sickle-cell disease«
- sickle-cell anemia«
- sickle-cell anaemia«
- severe combined immunodeficiency disease«
- severe combined immunodeficiency«
- pycnodysostosis«
- pseudohypertrophic dystrophy«
- phenylketonuria«
- pancreatic fibrosis«
- osteogenesis imperfecta«
- oculopharyngeal muscular dystrophy«
- neurofibromatosis«
- myotonic muscular dystrophy«
- myotonic dystrophy«
- myotonia atrophica«
- mucoviscidosis«
- malignant hyperthermia«
- lysinemia«
- lipochondrodystrophy«
- limb-girdle muscular dystrophy«
- infantile amaurotic idiocy«
- gargoylism«
- galactosemia«
- fibrocystic disease of the pancreas«
- familial hypercholesterolemia«
- dysostosis multiplex«
- drepanocytic anemia«
- drepanocytic anaemia«
- distal muscular dystrophy«
- diabetes«
- cystic fibrosis«
- crescent-cell anemia«
- crescent-cell anaemia«
- Wilson's disease«
- Spielmeyer-Vogt disease«
- McArdle's disease«
- Hirschsprung's disease«
- Fanconi's anemia«
- Fanconi's anaemia«
- Albers-Schonberg disease«
- Werdnig-Hoffman disease«
- Tay-Sachs disease«
- Tay-Sachs«
- Steinert's disease«
- Sachs disease«
- SCID«
- PKU«
- Niemann-Pick disease«
- Mediterranean anemia«
- Mediterranean anaemia«
- Marfan's syndrome«
- Hurler's syndrome«
- Hurler's disease«
- Huntington's disease«
- Huntington's chorea«
- Gaucher's disease«
- Duchenne's muscular dystrophy«
- Becker muscular dystrophy«