X linked recessive - Search results - Wiki X Linked Recessive
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X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be always expressed in... |
Sex linkage (redirect from X-linked) chromosome (autosome). In humans, these are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of all three differ... |
is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type. In medicine, X-linked dominant inheritance... |
[citation needed] The disorder is inherited in an X-linked recessive fashion (as the gene linked to it is on the X chromosome) and is almost entirely limited... |
synapses from functioning. CMT can also be produced by X-linked mutations and is named X-linked CMT (CMTX). In CMTX, mutated connexons create nonfunctional... |
X-linked intellectual disability refers to medical disorders associated with X-linked recessive inheritance that result in intellectual disability. As... |
Genetic disorder (redirect from X-linked syndrome) The divisions between recessive and dominant types are not "hard and fast", although the divisions between autosomal and X-linked types are (since the... |
Ichthyosis (redirect from Autosomal recessive congenital ichthyosis) underlying genetic cause and mode of inheritance (e.g., dominant, recessive, autosomal or X-linked). Ichthyosis comes from the Greek ἰχθύς ichthys, literally... |
(TATA-binding protein-associated factor 1) gene at Xq13.1. It has an X-linked, recessive pattern of inheritance. Genetic analysis suggests that the responsible... |
X-linked ichthyosis (abbreviated XLI) is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000... |
X-linked recessive hypoparathyroidism is a rare, congenital form of hypoparathyroidism. The signs and symptoms of X-linked recessive hypoparathyroidism... |
Spinocerebellar ataxia (redirect from X-linked recessive spinocerebellar ataxia) hereditary ataxias can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner.[citation needed] Many types of autosomal dominant cerebellar... |
Obligate carrier (section X-linked Recessive) an autosomal recessive and X-linked recessive manner. In X-linked recessive disorders, only females can be the carriers of the recessive mutation, making... |
Muscular dystrophy (redirect from X-linked Duchenne/Becker) during early development. Muscular dystrophies may be X-linked recessive, autosomal recessive, or autosomal dominant. Diagnosis often involves blood... |
inherited in an X-linked recessive pattern, called x-linked hypohidrotic ectodermal dysplasia (XLHED). A condition is considered X-linked if the mutated... |
Dominance (genetics) (redirect from Recessive allele) while those on sex chromosomes (allosomes) are termed X-linked dominant, X-linked recessive or Y-linked; these have an inheritance and presentation pattern... |
Leukodystrophy (section X-linked adrenoleukodystrophy) 7,600. The majority of types involve the inheritance of an X-linked recessive, or X-linked dominant trait, while others, although involving a defective... |
Rosy-faced lovebird colour genetics (category Commons category link is locally defined) genetic categories of dominant, co-dominant, recessive, and X-linked recessive (also called "sex-linked recessive"). While this seems fairly straightforward... |
Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) CMTX3 encoding protein Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) CT45A5: encoding protein... |
Hunter syndrome (category Commons category link from Wikidata) body tissues. Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. The symptoms of Hunter syndrome are comparable to those... |