moderate mental retardation

  • 11DSM-IV Codes (alphabetical) — Contents 1 A 2 B 3 C 4 D 5 E 6 F …

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  • 12Lujan-Fryns syndrome — Lujan–Fryns syndrome Classification and external resources Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin. ICD 10 F …

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  • 13Rosemary Kennedy — Infobox Person name = Rosemary Kennedy caption = birth date = September 13, 1918 birth place = Brookline, Massachusetts, USA death date = death date and age|mf=yes|2005|1|7|1918|9|13 death place = Fort Atkinson, Wisconsin, USA spouse = parents =… …

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  • 14Mucopolysaccharidosis — MPS I redirects here. For zhuyin or bopomofo, a phonetic system for romanizing Chinese, also known as Mandarin Phonetic Symbols I, see Bopomofo. Mucopolysaccharidosis Classification and external resources ICD 10 E76 ICD 9 …

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  • 15List of psychology topics — This page aims to list all topics related to psychology. This is so that those interested in the subject can monitor changes to the pages by clicking on Related changes in the sidebar. It is also to see the gaps in Wikipedia s coverage of the… …

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  • 16Pachygyria — DiseaseDisorder infobox Name = Pachygyria ICD10 = ICD10|Q|04|3|q|00 ICD9 = Pachygyria (from the Greek pachy meaning thick or fat gyri) is a congenital malformation of the cerebral hemisphere. It results in unusually thick convolutions of the… …

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  • 17Lesch–Nyhan syndrome — Lesch Nyhan syndrome Classification and external resources ICD 10 E79.1 ICD 9 277.2 …

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  • 18mucolipidosis — Any of a group of lysosomal storage diseases in which symptoms of visceral and mesenchymal mucopolysaccharide, glycoprotein, oligosaccharide, or glycolipid storage are present; clinically, they bear a superficial resemblance to the mu …

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  • 19Williams syndrome — Wil·liams syndrome wil yəmz n a rare genetic disorder characterized esp. by hypercalcemia of infants, heart defects (as supravalvular aortic stenosis), characteristic facial features (as an upturned nose, long philtrum, wide mouth, full lips, and …

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  • 20Joubert syndrome — Infobox Disease Name = Joubert syndrome Caption = DiseasesDB = 30688 ICD10 = ICD10|Q|04|3|q|00 ICD9 = ICD9|742.2 ICDO = OMIM = 213300 MedlinePlus = eMedicineSubj = eMedicineTopic = Joubert syndrome is a rare genetic disorder that affects the area …

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