ichthyosis : Related Words Words similar in meaning to ichthyosis
- ichthyosis«
- xeroderma«
- xerodermia«
- xeroderma pigmentosum«
- ichthyoses«
- congenital disease«
- ichthyosis vulgaris«
- inherited disorder«
- type«
- genetic disorder«
- severity«
- genetic abnormality«
- skin disease«
- hereditary disease«
- skin«
- hereditary condition«
- wet tanned skin«
- inherited disease«
- plural ichthyoses«
- genetic disease«
- onset ichthyosis«
- genetic defect«
- normal dry skin«
- ichythosis«
- genetic simple ichthyoses«
- genetic ichthyosis«
- excess dead skin«
- emollient oil«
- congenital keratitis«
- ancient greek ἰχθύς«
- kal1 gene«
- different gene«
- isotretinoin therapy«
- ichthyosis acquisita«
- ocular surface disease«
- genetic skin disorder«
- harlequin type ichthyosis«
- diabetes«
- flaky skin«
- heterogeneous family«
- cream«
- exact diagnosis«
- diagnosis«
- ocular manifestation«
- condition«
- cutaneous neoplasm«
- systemic syndrome«
- symptom«
- kallmann syndrome«
- american bulldog«
- cairn terrier«
- common breed«
- retinoids«
- musculoskeletal«
- ichthys«
- keratitis«
- skin biopsy«
- popular breed«
- dry skin«
- jack russell terrier«
- topical application«
- propylene glycol«
- treatments«
- treatment method«
- sun exposure«
- u national institute«
- golden retriever«
- other animals«
- domestic dog«
- fish«
- damaging effect«
- similar symptom«
- lactic acid«
- confetti«
- genetic testing«
- llama«
- deafness«
- cutaneous condition«
- swim«
- bathing«
- arthritis«
- family history«
- types«
- sunlight«
- chicken«
- disorder«
- mouse«
- gene«
- cattle«
- exposure«
- physician«
- kid«
- dog«
- list«
- scale«
- treatment«
- instance«
- animal«
- application«
- report«
- attempt«
- appearance«
- note«
- achondroplasia«
- osteosclerosis congenita«
- congenital megacolon«
- dwarfism«
- polygenic disorder«
- polygenic disease«
- autosomal recessive disease«
- autosomal recessive defect«
- congenital pancytopenia«
- congenital afibrinogenemia«
- otosclerosis«
- monogenic disorder«
- monogenic disease«
- autosomal dominant disorder«
- autosomal dominant disease«
- nevoid elephantiasis«
- hepatolenticular degeneration«
- muscular dystrophy«
- dystrophy«
- porphyria«
- lactase deficiency«
- juvenile amaurotic idiocy«
- lactose intolerance«
- branched chain ketoaciduria«
- inborn error of metabolism«
- milk intolerance«
- marble bones disease«
- maple syrup urine disease«
- pachyderma«
- osteopetrosis«
- oligodontia«
- oligodactyly«
- nanism«
- mucopolysaccharidosis«
- hyperbetalipoproteinemia«
- chondrodystrophy«
- achondroplasty«
- abetalipoproteinemia«
- osteogenesis imperfecta«
- myotonic muscular dystrophy«
- myotonic dystrophy«
- neurofibromatosis«
- galactosemia«
- myotonia atrophica«
- sickle-cell disease«
- sickle-cell anemia«
- sickle-cell anaemia«
- fibrocystic disease of the pancreas«
- phenylketonuria«
- drepanocytic anaemia«
- crescent-cell anaemia«
- familial hypercholesterolemia«
- thalassemia«
- drepanocytic anemia«
- crescent-cell anemia«
- thalassaemia«
- pseudohypertrophic dystrophy«
- oculopharyngeal muscular dystrophy«
- limb-girdle muscular dystrophy«
- distal muscular dystrophy«
- severe combined immunodeficiency disease«
- severe combined immunodeficiency«
- infantile amaurotic idiocy«
- malignant hyperthermia«
- cystic fibrosis«
- pancreatic fibrosis«
- von Recklinghausen's disease«
- tyrosinemia«
- thrombasthenia«
- pycnodysostosis«
- mucoviscidosis«
- lysinemia«
- lipochondrodystrophy«
- gargoylism«
- dysostosis multiplex«
- 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«
- Marfan's syndrome«
- Hurler's syndrome«
- Duchenne's muscular dystrophy«
- Becker muscular dystrophy«
- Huntington's chorea«
- 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«
