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 Übersetzung für 'X-linked recessive' von Englisch nach Deutsch
biol.
X-linked recessive {adj}
X-chromosomal-rezessiv
4 Wörter
biol.med.
X-linked recessive inheritance
X-chromosomal-rezessiver Erbgang {m}
Teiltreffer
biol.
X-linked dominant {adj}
X-chromosomal-dominant
biol.med.
X-linked inheritance
X-chromosomale Vererbung {f}
biol.med.
X-linked dominant inheritance
X-chromosomal-dominanter Erbgang {m}
med.
X-linked agammaglobulinaemia <XLA> [Br.]
Bruton-Syndrom {n} [Agammaglobulinämie vom Bruton-Typ]
med.
X-linked agammaglobulinemia <XLA> [Am.]
Bruton-Syndrom {n} [Agammaglobulinämie vom Bruton-Typ]
med.
X-linked spinal muscular atrophy type 1 <SMAX1>
spinobulbäre Muskelatrophie {f} <SBMA> Typ Kennedy
med.
X-linked ichthyosis [ICD-10, Q80.1, V. 2015]
X-chromosomal-rezessive Ichthyosis {f} [ICD-10, Q80.1, V. 2015]
X-linked bulbo-spinal atrophy <SBMA> [Kennedy's disease] spinobulbäre Muskelatrophie {f} Typ Kennedy <SBMA>
recessive {adj}zurückweichend
44
recessive {adj}nachlassend
24
biol.
recessive {adj}
rezessiv
31
biol.
recessive {adj}
zurücktretend
10
biol.
recessive gene
rezessives Gen {n}
biol.
recessive allele
rezessives Allel {n}
biol.
autosomal recessive {adj}
autosomal-rezessiv
med.
autosomal recessive disease
autosomal-rezessiv vererbte Krankheit {f}
med.
autosomal recessive hereditary disorders
autosomal rezessiv erbliche Störungen {pl}
biol.med.
autosomal recessive inheritance <ARI>
autosomal-rezessiver Erbgang {m}
med.
autosomal recessive disorder <ARD>
autosomal-rezessiv vererbte Erkrankung {f}
med.
autosomal recessive agammaglobulinaemia <ARA> [Br.]
autosomal-rezessive Agammaglobulinämie {f} <ARA>
22 Übersetzungen
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Übersetzung für 'X-linked recessive' von Englisch nach Deutsch

X-linked recessive {adj}
X-chromosomal-rezessivbiol.

X-linked recessive inheritance
X-chromosomal-rezessiver Erbgang {m}biol.med.

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X-linked dominant {adj}
X-chromosomal-dominantbiol.
X-linked inheritance
X-chromosomale Vererbung {f}biol.med.
X-linked dominant inheritance
X-chromosomal-dominanter Erbgang {m}biol.med.
X-linked agammaglobulinaemia <XLA> [Br.]
Bruton-Syndrom {n} [Agammaglobulinämie vom Bruton-Typ]med.
X-linked agammaglobulinemia <XLA> [Am.]
Bruton-Syndrom {n} [Agammaglobulinämie vom Bruton-Typ]med.
X-linked spinal muscular atrophy type 1 <SMAX1>
spinobulbäre Muskelatrophie {f} <SBMA> Typ Kennedymed.
X-linked ichthyosis [ICD-10, Q80.1, V. 2015]
X-chromosomal-rezessive Ichthyosis {f} [ICD-10, Q80.1, V. 2015]med.
X-linked bulbo-spinal atrophy <SBMA> [Kennedy's disease]
spinobulbäre Muskelatrophie {f} Typ Kennedy <SBMA>
recessive {adj}
zurückweichend

nachlassend

rezessivbiol.

zurücktretendbiol.
recessive gene
rezessives Gen {n}biol.
recessive allele
rezessives Allel {n}biol.
autosomal recessive {adj}
autosomal-rezessivbiol.
autosomal recessive disease
autosomal-rezessiv vererbte Krankheit {f}med.
autosomal recessive hereditary disorders
autosomal rezessiv erbliche Störungen {pl}med.
autosomal recessive inheritance <ARI>
autosomal-rezessiver Erbgang {m}biol.med.
autosomal recessive disorder <ARD>
autosomal-rezessiv vererbte Erkrankung {f}med.
autosomal recessive agammaglobulinaemia <ARA> [Br.]
autosomal-rezessive Agammaglobulinämie {f} <ARA>med.
Anwendungsbeispiele Englisch
  • In the DC cases, about 35% cases are X-linked-recessive on the DKC1 locus and 5% cases are autosomal dominant on the TERT and TERC loci.
  • The authors suggest a genetic origin with an autosomal or X-linked recessive inheritance rather than resulting from early prenatal disturbances.
  • In the majority of cases it is inherited as an X-linked recessive trait, though there are cases which arise from spontaneous mutations.
  • The different presentations are complicated by the pattern of X-linked recessive inheritance.
  • In humans, these are termed X-linked recessive, X-linked dominant and Y-linked.

  • In humans, inheritance of X-linked recessive traits follows a unique pattern made up of three points.
  • OTC deficiency is inherited in an X-linked recessive manner, meaning males are more commonly affected than females.
  • The disorder is X-linked recessive. About two thirds of cases are inherited from a person's mother, while one third of cases are due to a new mutation.
  • Another rare cause of a decreased BUN is ornithine transcarbamylase deficiency, which is a genetic disorder inherited in an X-linked recessive pattern.
  • IPEX syndrome is inherited in males by an X-linked recessive process.

  • Hunter syndrome has two clinical subtypes and (since it shows X-linked recessive inheritance) is the only one of the mucopolysaccharidoses in which the mother alone can pass the defective gene to a son.
  • Almost all cases are X-linked recessive and caused by a mutation in the retinoschisin gene ("RS1").
  • It is an X-linked recessive disorder that results in defective glucose-6-phosphate dehydrogenase enzyme.
  • Muscular dystrophies may be X-linked recessive, autosomal recessive, or autosomal dominant.
  • The inheritance pattern of VWD type 3 is autosomal recessive, while the inheritance pattern of hemophilia A is X-linked recessive.

  • All urea cycle defects, except OTC deficiency, are inherited in an autosomal recessive manner.
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