Class information for:
Level 1: BETA KETOTHIOLASE DEFICIENCY//ACETOACETYL COA SYNTHETASE//3 HYDROXY 3 METHYLGLUTARIC ACIDURIA

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
21433 360 24.8 62%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1351 7837 MAPLE SYRUP URINE DISEASE//METHYLMALONIC ACIDEMIA//JOURNAL OF INHERITED METABOLIC DISEASE

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 BETA KETOTHIOLASE DEFICIENCY Author keyword 38 93% 4% 14
2 ACETOACETYL COA SYNTHETASE Author keyword 31 92% 3% 12
3 3 HYDROXY 3 METHYLGLUTARIC ACIDURIA Author keyword 30 100% 3% 12
4 MITOCHONDRIAL ACETOACETYL COA THIOLASE Author keyword 27 92% 3% 11
5 3 KETOTHIOLASE DEFICIENCY Author keyword 17 100% 2% 8
6 HMG COA LYASE Author keyword 12 86% 2% 6
7 T2 DEFICIENCY Author keyword 11 100% 2% 6
8 3 HYDROXY 3 METHYLGLUTARYL COA LYASE DEFICIENCY Author keyword 9 83% 1% 5
9 HMG COA LYASE DEFICIENCY Author keyword 8 100% 1% 5
10 HMGCL Author keyword 8 100% 1% 5

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 BETA KETOTHIOLASE DEFICIENCY 38 93% 4% 14 Search BETA+KETOTHIOLASE+DEFICIENCY Search BETA+KETOTHIOLASE+DEFICIENCY
2 ACETOACETYL COA SYNTHETASE 31 92% 3% 12 Search ACETOACETYL+COA+SYNTHETASE Search ACETOACETYL+COA+SYNTHETASE
3 3 HYDROXY 3 METHYLGLUTARIC ACIDURIA 30 100% 3% 12 Search 3+HYDROXY+3+METHYLGLUTARIC+ACIDURIA Search 3+HYDROXY+3+METHYLGLUTARIC+ACIDURIA
4 MITOCHONDRIAL ACETOACETYL COA THIOLASE 27 92% 3% 11 Search MITOCHONDRIAL+ACETOACETYL+COA+THIOLASE Search MITOCHONDRIAL+ACETOACETYL+COA+THIOLASE
5 3 KETOTHIOLASE DEFICIENCY 17 100% 2% 8 Search 3+KETOTHIOLASE+DEFICIENCY Search 3+KETOTHIOLASE+DEFICIENCY
6 HMG COA LYASE 12 86% 2% 6 Search HMG+COA+LYASE Search HMG+COA+LYASE
7 T2 DEFICIENCY 11 100% 2% 6 Search T2+DEFICIENCY Search T2+DEFICIENCY
8 3 HYDROXY 3 METHYLGLUTARYL COA LYASE DEFICIENCY 9 83% 1% 5 Search 3+HYDROXY+3+METHYLGLUTARYL+COA+LYASE+DEFICIENCY Search 3+HYDROXY+3+METHYLGLUTARYL+COA+LYASE+DEFICIENCY
9 HMG COA LYASE DEFICIENCY 8 100% 1% 5 Search HMG+COA+LYASE+DEFICIENCY Search HMG+COA+LYASE+DEFICIENCY
10 HMGCL 8 100% 1% 5 Search HMGCL Search HMGCL

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 3 KETOTHIOLASE DEFICIENCY 54 83% 8% 30
2 ISOLEUCINE CATABOLISM 38 89% 5% 17
3 BETA KETOTHIOLASE DEFICIENCY 29 88% 4% 14
4 COENZYME A LYASE 28 69% 7% 24
5 A THIOLASE 23 100% 3% 10
6 HL GENE 17 100% 2% 8
7 COA THIOLASE 15 88% 2% 7
8 T2 DEFICIENCY 14 100% 2% 7
9 SUCCINYL COA 13 47% 6% 21
10 HUMAN 3 HYDROXY 3 METHYLGLUTARYL COA LYASE 12 86% 2% 6

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Molecular genetics of HMG-CoA lyase deficiency 2007 15 64 86%
Inborn errors of isoleucine degradation: A review 2006 24 51 33%
Molecular basis of 3-hydroxy-3-methylglutaric aciduria 2003 6 39 85%
MEDICAL ASPECTS OF KETONE-BODY METABOLISM 1995 108 85 24%
Ketone body metabolism and cardiovascular disease 2013 14 203 14%
3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A LYASE DEFICIENCY - REVIEW OF 18 REPORTED PATIENTS 1988 64 28 71%
Inborn errors of ketone body utilization 2015 0 53 70%
Pseudomonas mevalonii 3-hydroxy-3-methylglutaryl-CoA lyase 2000 2 13 85%
3-HYDROXY-3-METHYLGLUTARYL-COENZYME A LYASE DEFICIENCY - A REVIEW 1986 50 13 92%
Human 3-hydroxy-3-methylglutaryl-CoA lyase 2000 0 13 85%

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 CLIN GENET FUNCT GENOM 4 75% 0.8% 3
2 PEDIAT CLIN BIOCHEM 1 50% 0.6% 2
3 UNIT CLIN GENET FUNCT GENOM 1 25% 1.1% 4
4 INBORN ERRORS METAB IBC 1 33% 0.6% 2
5 CANADIAN NETWORK EXCELLENCE HUMAN GENET 1 50% 0.3% 1
6 INBORN ERRORS METAB SERV 1 50% 0.3% 1
7 MURDOCH CHILDRENS METAB SERV 1 50% 0.3% 1
8 REFERENCE MALAD HEREDITAI 1 50% 0.3% 1
9 HEREDITARY METAB DIS 0 33% 0.3% 1
10 PATOL METAB 0 33% 0.3% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000226901 L 3 HYDROXYBUTYRATE//FID GC FID//ACETOACETATE ESTERS
2 0.0000142115 3 HYDROXYISOBUTYRATE DEHYDROGENASE//HIBCH//SERINE DEHYDROGENASE
3 0.0000113729 MCAD DEFICIENCY//MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY//UNIT MOL MED
4 0.0000102319 D BETA HYDROXYBUTYRATE DEHYDROGENASE//D 3 HYDROXYBUTYRATE DEHYDROGENASE//HYDROXYBUTYRATE DEHYDROGENASE
5 0.0000102030 HEPATOCYTE MOUSE//D ERYTHRULOSE REDUCTASE//CELL MEDIUM
6 0.0000096638 METHYLMALONIC ACIDEMIA//PROPIONIC ACIDEMIA//METHYLMALONIC ACIDURIA
7 0.0000094007 MEVALONIC ACID//MEVALONATE 5 PYROPHOSPHATE DECARBOXYLASE//COMM HUMAN NUTR NUTRIT BIOL
8 0.0000092108 ELECTRON TRANSFERRING FLAVOPROTEIN//ACYL COA DEHYDROGENASE//2 4 DIENOYL COA REDUCTASE
9 0.0000091720 CARNITINE PALMITOYLTRANSFERASE//CARNITINE PALMITOYLTRANSFERASE DEFICIENCY//MITOCHONDRIAL HMG COA SYNTHASE
10 0.0000067033 FOOD FUS COMPLEX//KARMELLAE//HYPOCHOLESTEROLEMIC PEPTIDE