... JMP large multifunctional peptidase 7 LMP7 low molecular mass protein 7 low molecular weight protein 7 macropain subunit C13 multicatalytic endopeptidase complex ...

... Condition B27 C21orf61 FALP fat cell-specific low molecular weight protein fat tissue-specific low MW protein GCCD2 ...

SLC35A2-congenital disorder of glycosylation (SLC35A2-CDG, formerly known as congenital disorder of glycosylation type IIm) is an inherited condition that causes ...

... elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Pediatr Res. 2003 Aug;54( ... children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening. Pediatr Res. 2006 Sep;60( ...

... elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Pediatr Res. 2003 Aug;54( ... children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening. Pediatr Res. 2006 Sep;60( ...

... up to twice the usual amount of muscle mass in their bodies. They also tend to have ... in each cell (homozygotes) have significantly increased muscle mass and strength. People with a variant in one ...

... mutations in osteoporosis-pseudoglioma syndrome and high-bone-mass disorders. Joint Bone Spine. 2005 May;72(3): ... gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet. 2002 Jan;70( ...

... the FBN1 gene can cause another condition called MASS syndrome. This condition involves abnormalities in several parts ... PubMed FIBRILLIN 1; FBN1 STIFF SKIN SYNDROME; SSKS MASS SYNDROME NCBI Gene ClinVar Ades LC, Sullivan K, ...

... recurrent hydatidiform mole. A hydatidiform mole is a mass that forms early in pregnancy and is made ...