abetalipoproteinemia vs hereditary condition
hereditary condition vs abetalipoproteinemiaabetalipoproteinemia and hereditary condition both are nouns.
| Word | Noun | Adjective | Verb | Adverb |
|---|---|---|---|---|
| abetalipoproteinemia | Yes | No | No | No |
| hereditary condition | Yes | No | No | No |
As nouns,
hereditary condition is a hypernym of
abetalipoproteinemia; that is, hereditary condition is a
word with a broader meaning than abetalipoproteinemia:
- abetalipoproteinemia: a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels
- hereditary condition: a disease or disorder that is inherited genetically
Other hypernyms of abetalipoproteinemia include
congenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary disease, inherited disease, inherited disorder, hypobetalipoproteinemia, lipidosis.
| abetalipoproteinemia (noun) | hereditary condition (noun) |
|---|---|
| a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels | a disease or disorder that is inherited genetically |
Words related to "abetalipoproteinemia"
Words related to "hereditary condition"
- 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 abnormality
- genetic defect
- genetic disease
- genetic disorder
- hepatolenticular degeneration
- 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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