UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M M0 M1 M2 M4 M5 M7 M8 M9 MA MB MC MD ME MF MG MH MI MK ML MM MN MO MP MR MS MT MU MV MY
ME ME ME2 MEA MEB MEC MED MEE MEF MEG MEI MEL MEM MEN MEP MEQ MER MES MET MEV MEX MEZ

Mental retardation

[subnormal intellectual functioning which originates during the developmental period; multiple potential etiologies, including genetic defects and perinatal insults; intelligence quotient (IQ) scores are commonly used to determine whether an individual is mentally retarded; IQ scores between 70 and 79 are in the borderline mentally retarded range and scores below 67 are in the retarded range.(CSP)]
UMLS (ICPC) C0025362
E. Mental retardation; Basq. ATZERAPEN MENTALA; Da. Psykisk udviklingshaemning; Du. Mentale retardatie/intell achterst; Finn. KEHITYSVAMMAISUUS; Fr. Arrieration mentale; G. mentale Retardierung/Minderbegabung; Heb. pigur sixli; Hung. szellemi visszamaradottsag; It. Ritardo mentale; Norw. PSYKISK UTVIKLINGSHEMMET - f70 - f71 - f72 - f73 - f78 - f79; Port.Eu. Atraso mental; Sp. Retraso mental; Sw. FORSTANDSHANDIKAPP 
Finding
Mental or Behavioral Dysfunction
Relation/PAR: mental disorder; Diagnosis/Diseases Component; Mental Disorders Diagnosed in Childhood; Neurobehavioral Manifestations; PSYCHOLOGICAL;
Relation/CHD: Down syndrome; FRAGILE X SYNDROME; familial splenic anemia; cystathionine synthase deficiency; HD; Hypogonadotropic Hypogonadism; hypoxanthine guanine phosphoribosyltransferase deficiency; branched chain ketoaciduria; hereditary ceroid lipofuscinosis; cerebrooculorenal syndrome; phenylalaninemia; Prader Willi syndrome; Bourneville's disease; Angelman syndrome; histidinemia; orotate phosphoribosyltransferase deficiency; Smith Magenis syndrome;

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