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Chemical nomenclature, replete as it is with compounds with very complex names, is a repository for some names that may be considered unusual. A browse through the Physical Constants of Organic Compounds in the CRC Handbook of Chemistry and Physics (a fundamental resource) will reveal not just the whimsical work of chemists, but the sometimes peculiar compound names that occur as the ...
List of autoimmune diseases. Dermatosis in Crohn's disease. Demyelination in MS. PAS stain of lupus nephritis. Autoimmune urticaria. Proptosis in Graves' disease. This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the ...
Here are some ideas for rare boy names to help you find a name as one-of-a-kind as your baby boy. Rome. Flynn. Everest. Quinn. Caspian. Orson. Fisher. Montgomery. Hendrix. Dallas. Ulysses. Darius ...
Rare species. A rare species is a group of organisms that are very uncommon, scarce, or infrequently encountered. This designation may be applied to either a plant or animal taxon, and is distinct from the term endangered or threatened. Designation of a rare species may be made by an official body, such as a national government, state, or province.
Drosophila gene. Lunatic Fringe, Manic Fringe, and Radical Fringe. MAP kinase kinase kinase and MAP kinase kinase kinase kinase. MinosPhrime [5] Named after Minos Prime from the video game ULTRAKILL. Found in flower beds outside of college dormitory building, dug 2 inches deep into the soil. Soil was woodchip-heavy.
A rare disease is a disease that affects a small percentage of the population. In some parts of the world, the term orphan disease describes a rare disease whose rarity results in little or no funding or research for treatments, without financial incentives from governments or other agencies. Orphan drugs are medications targeting orphan ...
Progeria is a specific type of progeroid syndrome, also known as Hutchinson–Gilford syndrome or Hutchinson–Gilford progeroid syndrome (HGPS). [8] A single gene mutation is responsible for causing progeria. The affected gene, known as lamin A (LMNA), makes a protein necessary for holding the cell nucleus together.
Roberts syndrome, or sometimes called pseudothalidomide syndrome, is an extremely rare autosomal recessive genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs. It is caused by a mutation in the ESCO2 gene. It is one ...