dwarfism
61Miniature horse — at show in Europe Distinguishing features Small size, with horse phenotype 34–38 inches (86–97 cm) as measured at the last hairs of the mane Alternative names Mini horse Common nicknames …
62Seckel syndrome — A birth defect syndrome with severe short stature and, characteristically, low birth weight, very small head (microcephaly), receding forehead, large eyes, low ears, prominent beaklike protrusion of the nose, and smallish chin. Defects of bones… …
63Ellis–van Creveld syndrome — Classification and external resources Polydactyly in Ellis–van Creveld syndrome ICD 10 Q …
64Achondroplasia — Classification and external resources Jason Acuña, alias Wee Man , a star of Jackass …
65Chondrodystrophy — Classification and external resources ICD 10 Q78.9 ICD 9 756.4 …
66Europasaurus — Taxobox | name = Europasaurus fossil range = Upper Jurassic image width = 200px image caption = Life restoration of Europasaurus holgeri . regnum = Animalia phylum = Chordata classis = Sauropsida superordo = Dinosauria ordo = Saurischia subordo …
67Список наследственных заболеваний — Список генетических заболеваний Основные статьи: наследственные заболевания, Наследственные болезни обмена веществ, Ферментопатия. В большинстве случаев приведен также код, указывающий на тип мутации и связанные с ней хромосомы. См. также система …
68Angus cattle — This article is about Scottish Cattle. For other uses of the name Angus, see Angus (disambiguation). Black Angus redirects here; for the steakhouse see Black Angus Steakhouse Mixed herd of Black and Red Angus Angus cattle (Aberdeen Angus) are a… …
69Ellis-van Creveld syndrome — Infobox Disease Name = Ellis van Creveld syndrome Caption = Polydactyly in Ellis van Creveld syndrome DiseasesDB = 29309 ICD10 = ICD10|Q|77|6|q|65 ICD9 = ICD9|756.55 ICDO = OMIM = 225500 MedlinePlus = 001667 eMedicineSubj = ped eMedicineTopic =… …
70Nanism — Once known as dwarfism, this condition is now correctly called short stature. * * * Obsolete term for dwarfism. [G. nanos; L. nanus, dwarf] mulibrey n. (mu′li bra) autosomal recessive disorder with defects of liver, brain, muscle, and eyes. [from …
