WordNet

requiring or amenable to treatment by medicine especially as opposed to surgery; "medical treatment"; "pneumonia is a medical disease"
relating to the study or practice of medicine; "the medical profession"; "a medical student"; "medical school"
practices one branch of medicine (同)medical specialist
an expert who is devoted to one occupation or branch of learning (同)specializer, specialiser
the biological process whereby genetic factors are transmitted from one generation to the next
the total of inherited attributes (同)genetic endowment
any of several Old World herbs of the genus Medicago having small flowers and trifoliate compound leaves (同)medick, trefoil

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1. 小児および思春期における自閉症スペクトラム障害：マネージメントの概要 autism spectrum disorder in children and adolescents overview of management
2. 他の病状に影響を与える心理的要因：臨床的特徴、評価、および診断 psychological factors affecting other medical conditions clinical features assessment and diagnosis
3. 成人外傷患者における入院前のケア prehospital care of the adult trauma patient
4. 小児に対する入院前ケアの留意事項 pediatric considerations in prehospital care
5. 胸腔鏡の概要 an overview of medical thoracoscopy

GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder.

Shamseldin HE1, Bennett AH2, Alfadhel M3, Gupta V4, Alkuraya FS5,6.
Human genetics.Hum Genet.2016 Feb;135(2):245-51. doi: 10.1007/s00439-015-1632-8. Epub 2016 Jan 7.
Golgi apparatus (GA) is a membrane-bound organelle that serves a multitude of critical cellular functions including protein secretion and sorting, and cellular polarity. Many Mendelian diseases are caused by mutations in genes encoding various components of GA. GOLGA2 encodes GM130, a necessary comp
PMID 26742501

Exome-based case-control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy.

Shtir C1, Aldahmesh MA2, Al-Dahmash S3, Abboud E4, Alkuraya H5, Abouammoh MA3, Nowailaty SR6, Al-Thubaiti G6, Naim EA2,7, ALYounes B2,7, Binhumaid FS2,7, ALOtaibi AB7,8, Altamimi AS7,8, Alamer FH7,8, Hashem M2, Abouelhoda M7, Monies D2,7, Alkuraya FS9,10.
Human genetics.Hum Genet.2016 Feb;135(2):193-200. doi: 10.1007/s00439-015-1624-8. Epub 2015 Dec 22.
Diabetic retinopathy (DR) is a common clinical expression of diabetes mellitus-induced vasculopathy and is a major cause of vision loss. Significant gaps remain in our understanding of the molecular pathoetiology of DR, and it is hoped that human genetic approaches can reveal novel targets especiall
PMID 26693933

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.

Al-Hassnan ZN1,2,3,4, Shinwari ZM5, Wakil SM6, Tulbah S7, Mohammed S8, Rahbeeni Z9, Alghamdi M10, Rababh M11, Colak D12, Kaya N13, Al-Fayyadh M14,15, Alburaiki J16.
BMC medical genetics.BMC Med Genet.2016 Jan 14;17(1):3. doi: 10.1186/s12881-016-0267-5.
BACKGROUND: Familial dilated cardiomyopathy (DCM) is genetically heterogeneous. Mutations in more than 40 genes have been identified in familial cases, mostly inherited in an autosomal dominant pattern. DCM due to recessive mutations is rarely observed. In consanguineous families, homozygosity mappi
PMID 26768247