Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus...
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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...
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(see: gene interactions, polygenic inheritance, oligogenic inheritance). OMIM (Online Mendelian Inheritance in Man) is a comprehensive database of human...
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2021. Online Mendelian Inheritance in Man (OMIM): 146200 Online Mendelian Inheritance in Man (OMIM): 145980 Online Mendelian Inheritance in Man (OMIM):...
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Dominance (genetics) (redirect from Mendelian recessive disorder)
Newfoundland. Online Mendelian Inheritance in Man (OMIM): Hemoglobin—Beta Locus; HBB - 141900 — Sickle-Cell Anemia Online Mendelian Inheritance in Man (OMIM):...
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Variation in". Online Mendelian Inheritance in Man. Johns Hopkins University. 117800. Archived from the original on 30 April 2017. "Mendelian Traits in Humans"...
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Mendelian traits in humans are human traits that are substantially influenced by Mendelian inheritance. Most – if not all – Mendelian traits are also...
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Genetic disorder (redirect from Mendelian disorder)
Retrieved 2023-02-20. Public Health Genomics at CDC OMIM — Online Mendelian Inheritance in Man, a catalog of human genes and genetic disorders Genetic and...
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Victor A. McKusick (category Deaths from cancer in Maryland)
remained chief editor of Mendelian Inheritance in Man (MIM) and its online counterpart Online Mendelian Inheritance in Man (OMIM). He is widely known...
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Inheritance in Man (OMIM): 106210 AN Online Mendelian Inheritance in Man (OMIM): 106220 Aniridia and absent patella Online Mendelian Inheritance in Man...
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Online Mendelian Inheritance in Man (OMIM): Transglutaminase 3; TGM3 - 600238 "PADI3 gene". medlineplus.gov. MedlinePlus Genetics. Online Mendelian Inheritance...
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- 123700 Online Mendelian Inheritance in Man (OMIM): Cutis Laxa, Autosomal Recessive, Type II - 219200 Online Mendelian Inheritance in Man (OMIM): Cutis...
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Gland Secretion, Variation in". Online Mendelian Inheritance in Man. Johns Hopkins University. 117800. "Mendelian Traits in Humans" (PDF). Human Genetics...
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PMID 19061985. Online Mendelian Inheritance in Man (OMIM): 603632 Online Mendelian Inheritance in Man (OMIM): 603701 Online Mendelian Inheritance in Man (OMIM):...
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Gregor Mendel (redirect from Mendelian paradox)
established many of the rules of heredity, now referred to as the laws of Mendelian inheritance. Mendel worked with seven characteristics of pea plants: plant height...
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Leigh syndrome (category Neurological disorders in children)
1186/1750-1172-9-52. ISSN 1750-1172. PMC 4021638. PMID 24731534. Online Mendelian Inheritance in Man (OMIM): Leigh Syndrome - 256000 Pronicki, M; Matyja, E;...
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hereditary diseases. Data from Online Mendelian Inheritance in Man and medical literature were used to generate the terms currently in the HPO. The ontology contains...
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Citrullinemia (category Skin conditions resulting from errors in metabolism)
I citrullinemia (Online Mendelian Inheritance in Man (OMIM): 215700, also known as classic citrullinemia) usually becomes evident in the first few days...
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PMID 17668384. Online Mendelian Inheritance in Man (OMIM): 300203 Online Mendelian Inheritance in Man (OMIM): 609302 Online Mendelian Inheritance in Man (OMIM):...
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Infantile nephropathic- Online Mendelian Inheritance in Man (OMIM): 219800 Adolescent nephropathic- Online Mendelian Inheritance in Man (OMIM): 219900 Adult...
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neutrophil-expressed; ELANE. Online Mendelian Inheritance in Man. Johns Hopkins University. [1] WAS gene; WAS. Online Mendelian Inheritance in Man. Johns Hopkins University...
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Online Mendelian Inheritance in Man (OMIM): 311250 - hyperammonemia due to ornithine transcarbamylase deficiency Online Mendelian Inheritance in Man (OMIM):...
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S2CID 238859984. Online Mendelian Inheritance in Man (OMIM): Spinocerebellar Ataxia, Autosomal Recessive 1; SCAR1 - 606002 Online Mendelian Inheritance in Man (OMIM):...
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(25): e150. doi:10.1161/01.cir.100.25.e150. PMID 10604916. Online Mendelian Inheritance in Man (OMIM): Carney Complex, type 1; CNC1 - 160980 "Cardiac Myxoma"...
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Online Mendelian Inheritance in Man (OMIM): 103580 de Nanclares GP, Fernández-Rebollo E, Santin I, et al. (June 2007). "Epigenetic defects of GNAS in...
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54–62. doi:10.1038/ng1708. PMID 16369531. S2CID 8338877. Online Mendelian Inheritance in Man (OMIM): MATURITY-ONSET DIABETES OF THE YOUNG, TYPE VIII,...
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1159/000152813. PMID 976995. Online Mendelian Inheritance in Man (OMIM): 110900 - OMIM entry for Kell protein Online Mendelian Inheritance in Man (OMIM): 314850 -...
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Pemphigoid~clinical at eMedicine Online Mendelian Inheritance in Man (OMIM): DYSTONIN; DST - 113810 Online Mendelian Inheritance in Man (OMIM): COLLAGEN, TYPE XVII...
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[1] Online Mendelian Inheritance in Man (OMIM): 607596 Online Mendelian Inheritance in Man (OMIM): 614678 Online Mendelian Inheritance in Man (OMIM): 615851...
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thumb" is the common term preferred by the online database Online Mendelian Inheritance in Man and was first used in a 1965 study. Stub thumbs have also been...
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