Hypoglossia
Classification and external resources
ICD-10	Q38.3

Hypoglossia is a short, incompletely developed tongue. It can occur either as an isolated malformation or in association with other deformities,^[1] particularly limb defects in a syndrome known as oromandibular limb hypogenesis syndrome.

[edit] References

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v • d • e Congenital malformations and deformations of digestive system (Q35-Q45, 749-751) Upper GI tract Tongue, mouth and pharynx Cleft lip and palate · Van der Woude syndrome · tongue (Ankyloglossia, Macroglossia, Hypoglossia) Esophagus EA/TEF (Esophageal atresia: types A, B, C, and D, Tracheoesophageal fistula: types B, C, D and E) esophageal rings (Esophageal web  · upper, Schatzki ring · lower) Stomach Pyloric stenosis · Hiatus hernia Lower GI tract Intestines Intestinal atresia (Duodenal atresia) · Meckel's diverticulum · Hirschsprung's disease · Intestinal malrotation · Dolichocolon · Enteric duplication cyst Rectum/anus Imperforate anus · Persistent cloaca Accessory Pancreas Annular pancreas · Accessory pancreas · Johanson-Blizzard syndrome Pancreas divisum Bile duct Choledochal cysts (Caroli disease) · Biliary atresia Liver Alagille syndrome mouth navs: anat/dev, noncongen/congen face/congen GI/neoplasia, symptoms, proc digestive system navs: anat of tract,glands,perit,diaphragm/physio/dev, noncongen/congen/congen of d+w/neoplasia, symptoms+signs/eponymous, proc

Do not confuse hypoglossia with hypolockgheai, which is a disability to shoot something spherical into something over ten feet tall.