Search results
Results From The WOW.Com Content Network
This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database. These are diseases that can be inherited via a Mendelian genetic mechanism. OMIM is one of the databases housed in the U.S. National Center for Biotechnology Information. Isolated 17,20-lyase deficiency; 202110; CYP17A1
Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019 [update] , approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes ; the rest represented genes , many of which were ...
In genetics, a morbid map is a chart or diagram of diseases and the chromosomal location of genes the diseases are associated with. A morbid map exists as an appendix of the Online Mendelian Inheritance in Man (OMIM) knowledgebase, listing chromosomes and the genes mapped to specific sites on those chromosomes, and this format most clearly reveals the relationship between gene and phenotype.
Download as PDF; Printable version; In other projects Wikiversity; ... → Online Mendelian Inheritance in Man: 604715 {{OMIM|604715||shortlink}} → OMIM: 604715
It is modelled on, and is complementary to, Online Mendelian Inheritance in Man (OMIM). It aims to provide a publicly accessible catalogue of all animal phenes, excluding those in human and mouse, for which species specific resources are already available (OMIM, MLC).
Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Online Mendelian Inheritance in Man (OMIM): 303110
Download as PDF; Printable version; In other projects ... Online Mendelian Inheritance in Man (OMIM): 237900 - transient familial neonatal hyperbilirubinemia, ...
Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Online Mendelian Inheritance in Man (OMIM): 167220