Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Aspartylglucosaminuria

An autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group (also called glycoproteinosis).

Abnormality of the ulna

An abnormality of the ulna bone of the forearm.

合計: 0

（表示件数）

PMID (PMCID)