muscular dystrophy vs genetic abnormality
genetic abnormality vs muscular dystrophymuscular dystrophy and genetic abnormality both are nouns.
| Word | Noun | Adjective | Verb | Adverb |
|---|---|---|---|---|
| muscular dystrophy | Yes | No | No | No |
| genetic abnormality | Yes | No | No | No |
As nouns,
genetic abnormality is a hypernym of
muscular dystrophy; that is, genetic abnormality is a
word with a broader meaning than muscular dystrophy:
- muscular dystrophy: any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles
- genetic abnormality: a disease or disorder that is inherited genetically
Other hypernyms of muscular dystrophy include
congenital disease, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder.
| muscular dystrophy (noun) | genetic abnormality (noun) |
|---|---|
| any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles | a disease or disorder that is inherited genetically |
Words related to "muscular dystrophy"
- Becker muscular dystrophy
- Duchenne's muscular dystrophy
- Steinert's disease
- congenital disease
- distal muscular dystrophy
- dystrophy
- genetic abnormality
- genetic defect
- genetic disease
- genetic disorder
- hereditary condition
- hereditary disease
- inherited disease
- inherited disorder
- limb-girdle muscular dystrophy
- myotonia atrophica
- myotonic dystrophy
- myotonic muscular dystrophy
- oculopharyngeal muscular dystrophy
- pseudohypertrophic dystrophy
Words related to "genetic abnormality"
- Albers-Schonberg disease
- Fanconi's anaemia
- Fanconi's anemia
- Hirschsprung's disease
- McArdle's disease
- Spielmeyer-Vogt disease
- Wilson's disease
- abetalipoproteinemia
- achondroplasia
- achondroplasty
- autosomal dominant disease
- autosomal dominant disorder
- autosomal recessive defect
- autosomal recessive disease
- branched chain ketoaciduria
- chondrodystrophy
- congenital afibrinogenemia
- congenital disease
- congenital megacolon
- congenital pancytopenia
- disease
- dwarfism
- dystrophy
- genetic defect
- genetic disease
- genetic disorder
- hepatolenticular degeneration
- hereditary condition
- hereditary disease
- hyperbetalipoproteinemia
- ichthyosis
- inborn error of metabolism
- inherited disease
- inherited disorder
- juvenile amaurotic idiocy
- lactase deficiency
- lactose intolerance
- maple syrup urine disease
- marble bones disease
- milk intolerance
- monogenic disease
- monogenic disorder
- mucopolysaccharidosis
- muscular dystrophy
- nanism
- nevoid elephantiasis
- oligodactyly
- oligodontia
- osteopetrosis
- osteosclerosis congenita
- otosclerosis
- pachyderma
- polygenic disease
- polygenic disorder
- porphyria
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