Übersetzung für 'X linked recessive' von Englisch nach Deutsch

X-linked recessive {adj}

X-chromosomal-rezessivbiol.

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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 disease

autosomal-rezessiv vererbte Krankheit {f}med.

autosomal recessive {adj} <AR>

autosomal-rezessiv <AR>biol.

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.

• 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.