hereditary condition

hereditary condition
noun
a disease or disorder that is inherited genetically
Syn:
Hypernyms: ↑disease
Hyponyms:
monogenic disorder, ↑monogenic disease, ↑polygenic disorder, ↑polygenic disease, ↑achondroplasia, ↑achondroplasty, ↑osteosclerosis congenita, ↑chondrodystrophy, ↑abetalipoproteinemia, ↑inborn error of metabolism, ↑Hirschsprung's disease, ↑congenital megacolon, ↑mucopolysaccharidosis, ↑hyperbetalipoproteinemia, ↑ichthyosis, ↑maple syrup urine disease, ↑branched chain ketoaciduria, ↑McArdle's disease, ↑muscular dystrophy, ↑dystrophy, ↑oligodactyly, ↑oligodontia, ↑otosclerosis, ↑autosomal dominant disease, ↑autosomal dominant disorder, ↑autosomal recessive disease, ↑autosomal recessive defect, ↑Fanconi's anemia, ↑Fanconi's anaemia, ↑congenital pancytopenia, ↑Spielmeyer-Vogt disease, ↑juvenile amaurotic idiocy, ↑congenital afibrinogenemia, ↑osteopetrosis, ↑Albers-Schonberg disease, ↑marble bones disease, ↑nevoid elephantiasis, ↑pachyderma, ↑dwarfism, ↑nanism, ↑lactose intolerance, ↑lactase deficiency, ↑milk intolerance, ↑porphyria, ↑hepatolenticular degeneration, ↑Wilson's disease

Useful english dictionary. 2012.

Игры ⚽ Поможем решить контрольную работу

Look at other dictionaries:

  • Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D …   Wikipedia

  • Hereditary fructose intolerance — DiseaseDisorder infobox Name = Fructose intolerance ICD10 = ICD10|E|74|1|e|70 ICD9 = ICD9|271.2 ICDO = Caption = Fructose OMIM = 229600 MedlinePlus = 000359 eMedicineSubj = ped eMedicineTopic = 988 DiseasesDB = 5003 MeshID = D005633 Hereditary… …   Wikipedia

  • hereditary */ — UK [həˈredət(ə)rɪ] / US [həˈredɪˌterɪ] adjective 1) biology a hereditary disease or quality is passed from a parent to a child in their genes Cystic fibrosis is a hereditary condition. 2) legal a hereditary title or right is officially passed… …   English dictionary

  • hereditary hypersegmentation of neutrophils — a hereditary condition in which the neutrophils are multilobed; called also Undritz anomaly …   Medical dictionary

  • hereditary disease — noun a disease or disorder that is inherited genetically • Syn: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑inherited disease, ↑inherited disorder, ↑ …   Useful english dictionary

  • Hereditary hemorrhagic telangiectasia — Classification and external resources Characteristic lip telangiectases. ICD 10 I …   Wikipedia

  • Hereditary multiple exostoses — Classification and external resources Photograph of the legs of a 26 year old male showing multiple lumps leading to deformity. ICD 10 Q …   Wikipedia

  • Hereditary nonpolyposis colorectal cancer — Classification and external resources ICD 10 C18 C20 ICD 9 …   Wikipedia

  • Hereditary equine regional dermal asthenia — (HERDA) aka hyperelastosis cutis (HC) is an inherited autosomal recessive connective tissue disorder. It develops from a homozygous recessive mutation that weakens collagen fibers that allow the skin of the animal to stay connected to the rest of …   Wikipedia

  • Hereditary persistence of fetal hemoglobin — (HPFH, BrE: Hereditary persistence of foetal haemoglobin ) is a benign condition in which significant fetal hemoglobin (hemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult type… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”