Class information for:
Level 1: CONGENITAL DISORDERS OF GLYCOSYLATION//CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME//CDG

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
14512 699 31.9 81%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1014 9854 CONGENITAL DISORDERS OF GLYCOSYLATION//GLYCOPROTEOMICS//OLIGOSACCHARYLTRANSFERASE

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CONGENITAL DISORDERS OF GLYCOSYLATION Author keyword 100 69% 12% 85
2 CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME Author keyword 91 85% 7% 47
3 CDG Author keyword 79 74% 8% 59
4 PMM2 Author keyword 38 93% 2% 14
5 CDG IA Author keyword 37 100% 2% 14
6 CONGENITAL DISORDER OF GLYCOSYLATION Author keyword 34 63% 5% 35
7 PHOSPHOMANNOMUTASE DEFICIENCY Author keyword 20 100% 1% 9
8 PHOSPHOMANNOMUTASE Author keyword 19 51% 4% 27
9 GLYCOBIOL CARBOHYDRATE CHEM PROGRAM Address 17 63% 2% 17
10 PMM2 CDG Author keyword 17 100% 1% 8

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 CONGENITAL DISORDERS OF GLYCOSYLATION 100 69% 12% 85 Search CONGENITAL+DISORDERS+OF+GLYCOSYLATION Search CONGENITAL+DISORDERS+OF+GLYCOSYLATION
2 CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME 91 85% 7% 47 Search CARBOHYDRATE+DEFICIENT+GLYCOPROTEIN+SYNDROME Search CARBOHYDRATE+DEFICIENT+GLYCOPROTEIN+SYNDROME
3 CDG 79 74% 8% 59 Search CDG Search CDG
4 PMM2 38 93% 2% 14 Search PMM2 Search PMM2
5 CDG IA 37 100% 2% 14 Search CDG+IA Search CDG+IA
6 CONGENITAL DISORDER OF GLYCOSYLATION 34 63% 5% 35 Search CONGENITAL+DISORDER+OF+GLYCOSYLATION Search CONGENITAL+DISORDER+OF+GLYCOSYLATION
7 PHOSPHOMANNOMUTASE DEFICIENCY 20 100% 1% 9 Search PHOSPHOMANNOMUTASE+DEFICIENCY Search PHOSPHOMANNOMUTASE+DEFICIENCY
8 PHOSPHOMANNOMUTASE 19 51% 4% 27 Search PHOSPHOMANNOMUTASE Search PHOSPHOMANNOMUTASE
9 PMM2 CDG 17 100% 1% 8 Search PMM2+CDG Search PMM2+CDG
10 PHOSPHOMANNOSE ISOMERASE 14 39% 4% 29 Search PHOSPHOMANNOSE+ISOMERASE Search PHOSPHOMANNOSE+ISOMERASE

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 DEFICIENT GLYCOPROTEIN SYNDROME 200 69% 25% 172
2 PHOSPHOMANNOSE ISOMERASE DEFICIENCY 115 83% 9% 66
3 CDG IA 106 95% 5% 36
4 PHOSPHOMANNOMUTASE DEFICIENCY 102 95% 5% 35
5 SYNDROME TYPE 1A 89 100% 4% 27
6 CDG 81 83% 6% 45
7 PMM2 73 89% 5% 33
8 GLYCOSYLATION TYPE IA 33 83% 3% 19
9 CDG SYNDROME 30 100% 2% 12
10 CONGENITAL DISORDERS 29 31% 11% 78

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Congenital Disorders of Glycosylation: An Update on Defects Affecting the Biosynthesis of Dolichol-Linked Oligosaccharides 2009 74 112 76%
The clinical spectrum of phosphomannomutase 2 deficiency (CDG-Ia) 2009 36 104 95%
Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction 2015 5 70 26%
Congenital disorders of glycosylation: A rapidly expanding disease family 2007 126 67 61%
Altered glycan structures: the molecular basis of congenital disorders of glycosylation 2005 139 56 63%
Congenital disorders of glycosylation: A review 2002 87 75 85%
Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge 2013 46 68 32%
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib 2009 24 22 91%
Genetic defects in the human glycome 2006 180 99 29%
Congenital disorders of glycosylation: review of their molecular bases, clinical presentations and specific therapies 2003 150 126 47%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 GLYCOBIOL CARBOHYDRATE CHEM PROGRAM 17 63% 2.4% 17
2 GENET DIS PROGRAM 8 52% 1.6% 11
3 KLIN POLIKLIN KINDER JUGENDMED ALLGEMEINE PAD 3 50% 0.6% 4
4 RIGSHOSP 4062 3 50% 0.6% 4
5 GENET METAB ENDOCRINE DIS 3 60% 0.4% 3
6 KINDERHEILKUNDE 1 3 60% 0.4% 3
7 SEKT METAB ENDOKRINOL ERKRANKUNGEN 3 60% 0.4% 3
8 AG PRAVENT KARDIOL 2 67% 0.3% 2
9 LEHRSTUHL ZELLBIOL PFLANZENBIOCHEM 2 67% 0.3% 2
10 UNITE GLYCOBIOL SIGNALISAT CELLULAIRE 2 67% 0.3% 2

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000149372 RHOMBENCEPHALOSYNAPSIS//PONTOCEREBELLAR HYPOPLASIA//GOMEZ LOPEZ HERNANDEZ SYNDROME
2 0.0000142704 DOLICHOL//POLYPRENOLS//POLYPRENOL
3 0.0000135168 CARBOHYDRATE DEFICIENT TRANSFERRIN//CDT//CARBOHYDRATE DEFICIENT TRANSFERRIN CDT
4 0.0000115528 UDP GALACTOSE TRANSPORTER//NUCLEOTIDE SUGAR TRANSPORTER//CMP SIALIC ACID TRANSPORTER
5 0.0000100505 UDP SUGAR HYDROLASE//PHOSPHOHEXOMUTASE//HAD SUPERFAMILY
6 0.0000096595 CONGENITAL DYSERYTHROPOIETIC ANEMIA//CONGENITAL DYSERYTHROPOIETIC ANAEMIA//HEMPAS
7 0.0000082609 TRANSALDOLASE DEFICIENCY//ESA 8080//NEONATAL HAEMORRHAGIC DIATHESIS
8 0.0000065095 OLIGOSACCHARYLTRANSFERASE//OLIGOSACCHARYL TRANSFERASE//STT3
9 0.0000064564 GLYCOPROTEOMICS//GLYCOMICS//GLYC GLYCOPROTE
10 0.0000061096 CUTIS LAXA//MID DERMAL ELASTOLYSIS//ANNULAR ELASTOLYTIC GIANT CELL GRANULOMA