- locus heterogeneity
- see genetic h.
Medical dictionary. 2011.
Medical dictionary. 2011.
genetic heterogeneity — the production of identical or similar phenotypes by more than one genetic mutation; either by different mutant alleles at the same locus (allelic h.) or by mutations at two or more loci (locus h.) … Medical dictionary
Allelic heterogeneity — The phenomenon in which different mutations at the same locus (or gene) cause the same disorder. For example,β thalessemia may be caused by several different mutations in the β globin gene … Wikipedia
Restless legs syndrome — Infobox Disease Name = Restless legs syndrome Caption = Sleep pattern of a Restless Legs Syndrome patient (red) vs. a healthy sleep pattern (blue). DiseasesDB = 29476 ICD10 = ICD10|G|25|8|g|20 ICD9 = ICD9|333.94 ICDO = OMIM = 102300 OMIM mult =… … Wikipedia
Heterogeneous — is an adjective used to describe an object or system consisting of multiple items having a large number of structural variations. It is the opposite of homogeneous , which means that an object or system consists of multiple identical items.… … Wikipedia
EFHC1 — EF hand domain (C terminal) containing 1, also known as EFHC1, is a human gene.cite web | title = Entrez Gene: EFHC1 EF hand domain (C terminal) containing 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
SPG3A — Spastic paraplegia 3A (autosomal dominant), also known as SPG3A, is a human gene.cite web | title = Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
FBXW4 — F box and WD repeat domain containing 4, also known as FBXW4, is a human gene.cite web | title = Entrez Gene: FBXW4 F box and WD repeat domain containing 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
Dysbindin — Dystrobrevin binding protein 1 Identifiers Symbols DTNBP1; DBND; DKFZp564K192; FLJ30031; HPS7; MGC20210; My031; SDY External IDs … Wikipedia
EXT1 — Exostoses (multiple) 1, also known as EXT1, is a human gene.cite web | title = Entrez Gene: EXT1 exostoses (multiple) 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2131| accessdate = ] PBB Summary… … Wikipedia
Genetic screen — This article is about a method to identify the functions of genes. For screening or testing for genetic diseases, see genetic testing. A genetic screen (often known as a phenotypic screen, or shortened to screen) is a procedure or test to… … Wikipedia