GGDonto/Entry

GGDonto: Genetic Glyco-Diseases Ontology

CON00388 : 'B4GALT7-CDG' 'Ehlers-Danlos syndrome, progeroid form' (Integration tree) (Synthesis tree)

Common disease names

B4GALT7-CDG
Ehlers-Danlos syndrome, progeroid form
Ehlers-Danlos syndrome, progeroid type, 1
Galactosyltransferase 1 deficiency

Full list of disease names

Preferred Term	EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1
Preferred Term ABBR	EDSP1
Synonyms (from OMIM and MeSH)	DERMATAN SULFATE PROTEOGLYCAN GALACTOSYLTRANSFERASE I DEFICIENCY PDS, DEFECTIVE BIOSYNTHESIS OF PROTEODERMATAN SULFATE, DEFECTIVE BIOSYNTHESIS OF Progeroid variant of Ehlers-Danlos syndrome XGPT DEFICIENCY XYLOSYLPROTEIN 4-BETA-GALACTOSYLTRANSFERASE DEFICIENCY

UMLS CUI

C1869122

UMLS SAB

MeSH (SCR)

UMLS CODE

C536201

OMIM DATA

Gene	B4GALT7
Gene Number	604327
Phenotype Number	130070

References

Concept

  Cummings RD, Pierce JM (eds) (2009) Handbook of Glycomics. Elsevier. ISBN:9780123736000. Freeze HH, Eklund E (2009) Introduction to Human Glycosylation Disorders. pp 431-464.
  Freeze HH (2006) Genetic defects in the human glycome. Nat Rev Genet 7(7):537-551. Table 3 Human diseases caused by genetic defects in O-glycosylation and glycolipid synthesis pathways.
  Freeze HH, Schachter H (2009) Genetic Disorders of Glycosylation. pp 585-600. Table 42.1 Genetic defects of glycan synthesis in humans.
  Hennet T (2012) Diseases of glycosylation beyond classical congenital disorders of glycosylation. Biochim Biophys Acta 1820(9):1306-1317.
  Hennet T (2012) Diseases of glycosylation beyond classical congenital disorders of glycosylation. Biochim Biophys Acta 1820(9):1306-1317. Table 1 Diseases of glycosylation.
  Jaeken J, Hennet T, Matthijs G, Freeze HH (2009) CDG nomenclature: Time for a change. Biochim Biophys Acta 1792(9):825-826. Table 1 Proposed nomenclature for CDG.

Relations

  Cummings RD, Pierce JM (eds) (2009) Handbook of Glycomics. Elsevier. ISBN:9780123736000. Freeze HH, Eklund E (2009) Introduction to Human Glycosylation Disorders. pp 431-464.
  Freeze HH (2006) Genetic defects in the human glycome. Nat Rev Genet 7(7):537-551.
  Jaeken J, Hennet T, Freeze HH, Matthijs G (2008) On the nomenclature of congenital disorders of glycosylation. J Inherit Metab Dis 31(6):669-672.
  Jaeken J, Hennet T, Matthijs G, Freeze HH (2009) CDG nomenclature: Time for a change. Biochim Biophys Acta 1792(9):825-826.
  Kamerling JP (ed) (2007) Comprehensive Glycoscience. From Chemistry to Systems Biology. Elsevier, Oxford. ISBN:9780444527462.
  Pagon RA, Bird TD, Dolan CR, Stephens K, Adam MP (eds) (1993-) GeneReviews. University of Washington, Seattle. ISSN:2372-0697. Sparks SE, Krasnewich DM (2014) Congenital Disorders of N-linked Glycosylation Pathway Overview. Initial Posting: 15 Aug 2005, Last Revision: 30 Jan 2014, Accessed 22 Feb 2016.
  Varki A, Cummings RD, Esko JD, Freeze HH, Stanley P, Bertozzi CR, Hart GW, Etzler ME (eds) (2009) Essentials of glycobiology, 2nd ed. Cold Spring Harbor Laboratory Press, New York. ISBN:9780879697709. Freeze HH (2009) Genetic disorders of glycan degradation. pp 567-583.