oligodactyly : Related Words Words similar in meaning to oligodactyly
- hypodactyly«
- oligodactyly«
- dactyly«
- ectrodactyly«
- toe«
- finger«
- inherited disorder«
- weyer ulnar ray syndrome«
- inherited disease«
- vadoma people«
- hereditary disease«
- hereditary condition«
- familial etiology«
- genetic disorder«
- ancient greek oligos meaning«
- genetic disease«
- foot«
- genetic defect«
- genetic abnormality«
- congenital disease«
- foot malformation«
- similar abnormality«
- bootmaking«
- central digit«
- dysmelia«
- daktylos«
- poland syndrome«
- extreme instance«
- hypoglycaemia«
- greek prefix«
- syndactyly«
- polydactyly«
- hypercholesterolemia«
- fine control«
- hand«
- scale«
- ring finger«
- extreme form«
- oligarchy«
- cab driver«
- daily activity«
- polygamy«
- medical condition«
- syndrome«
- claw«
- thumb«
- digit«
- opposite«
- zimbabwe«
- symptom«
- frequency«
- task«
- absence«
- people«
- sign«
- writing«
- presence«
- condition«
- type«
- porphyria«
- polygenic disorder«
- polygenic disease«
- pachyderma«
- otosclerosis«
- osteosclerosis congenita«
- osteopetrosis«
- oligodontia«
- 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«
- dwarfism«
- congenital pancytopenia«
- congenital megacolon«
- congenital afibrinogenemia«
- chondrodystrophy«
- branched chain ketoaciduria«
- autosomal recessive disease«
- autosomal recessive defect«
- autosomal dominant disorder«
- autosomal dominant disease«
- achondroplasty«
- achondroplasia«
- 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«
