List of Bratz charactersDyschromatosis symmetrica hereditaria: Dyschromatosis symmetrica hereditaria (also known as "Reticulate acropigmentation of Dohi," and "Symmetrical dyschromatosis of the extremities") is a rare autosomally inherited dermatosis. It is characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities.Acromelanism: Acromelanism is a genetically determined, temperature-dependent pigmentation pattern, with full expression only occurring on legs, ears, tail and face. Seen in Siamese and Himalayan cats, rats, and rabbits.Amelanism: Amelanism (also known as amelanosis) is a pigmentation abnormality characterized by the lack of pigments called melanins, commonly associated with a genetic loss of tyrosinase function. Amelanism can affect fish, amphibians, reptiles, birds, and mammals including humans.Melanosome: A melanosome is an organelle found in animal cells, and is the cellular site of synthesis, storage and transport of melanin, the most common light-absorbing pigment found in the animal kingdom. These melanosomes are responsible for color and photoprotection in animal tissues.MelanocyteIdiopathic eruptive macular pigmentation: Idiopathic eruptive macular pigmentation is a skin condition developing in young persons, with an average age of 11, characterized by asymptomatic widespread brown to gray macules of up to several centimeters in diameter on the neck, trunk, and proximal extremities.Dermal equivalent: The dermal equivalent is an in vitro model of the dermal layer of skin. It is constructed by seeding dermal fibroblasts into a collagen gel.Sunlight (cleaning product): Sunlight is a brand of household soap originally produced by the British company Lever Brothers in 1884. It was the world's first packaged, branded laundry soap.Deaf white catUVB-induced apoptosis: UVB-induced apoptosis is the programmed cell death of cells that become damaged by ultraviolet rays. This is notable in skin cells, to prevent melanoma.Progressive macular hypomelanosis: Progressive macular hypomelanosis is a common skin condition, a disorder, observed more frequently in young women with darkly pigmented skin who originate from or reside in tropical climates.Necrolytic acral erythema: Necrolytic acral erythema is a cutaneous condition that is a manifestation of hepatitis C viral infection or zinc deficiency.Idioteuthis cordiformis: Idioteuthis cordiformis is a species of whip-lash squid found in tropical regions of the west Pacific Ocean. The species is commonly known as the 'love-heart squid' because the species name cordiformis is Latin for 'heart shaped'.Hypovitaminosis DHuman hair color: Hair color is the pigmentation of hair follicles due to two types of melanin: eumelanin and pheomelanin. Generally, if more eumelanin is present, the colour of the hair is darker; if less eumelanin is present, the hair is lighter.Anticipation (genetics): In genetics, anticipation is a phenomenon whereby as a genetic disorder is passed on to the next generation, the symptoms of the genetic disorder become apparent at an earlier age with each generation. In most cases, an increase of severity of symptoms is also noted.Vitiligo Research FoundationAtrial myxoma: An atrial myxoma is a benign tumor of the heart, commonly found within the left and right atria on the interatrial septum.Vitamin DActinic elastosis: Actinic elastosis, also known as solar elastosis is an accumulation of abnormal elastin (elastic tissue) in the dermis of the skin, or in the conjunctiva of the eye, which occurs as a result of the cumulative effects of prolonged and excessive sun exposure, a process known as photoaging.Keratinocyte: A keratinocyte is the predominant cell type in the epidermis, the outermost layer of the skin, constituting 90% of the cells found there.List of inorganic pigments: The following list includes commercially or artistically important inorganic pigments of natural and synthetic origin. The only dyes listed are derived directly from inorganic pigments.Agouti gene: The Agouti gene is responsible for determining whether a mammal's coat is banded (agouti) or of a solid color (non-agouti). The chief product of the Agouti gene is Agouti signalling peptide (ASP), but there are a number of alternative splice products.Malformative syndrome: A malformative syndrome (or malformation syndrome) is a recognizable pattern of congenital anomalies that are known or thought to be causally related (VIIth International Congress on Human Genetics).Erythromelanosis follicularis faciei et colli: Erythromelanosis follicularis faciei et colli is an erythematous pigmentary disease involving the follicles, characterized by a reddish-brown, sharply demarcated, symmetrical discoloration involving the preauricular and maxillary regions.James, William; Berger, Timothy; Elston, Dirk (2005).Selection (relational algebra): In relational algebra, a selection (sometimes called a restriction to avoid confusion with SQL's use of SELECT) is a unary operation written asOculocutaneous albinism type I: Oculocutaneous Albinism Type I or –Type 1A (OCA1A) is an autosomal recessive skin disease associated with albinism. This type of albinism is caused when the gene OCA1 does not function properly.WGAViewer: WGAViewer is a bioinformatics software tool which is designed to visualize, annotate, and help interpret the results generated from a genome wide association study (GWAS). Alongside the P values of association, WGAViewer allows a researcher to visualize and consider other supporting evidence, such as the genomic context of the SNP, linkage disequilibrium (LD) with ungenotyped SNPs, gene expression database, and the evidence from other GWAS projects, when determining the potential importance of an individual SNP.