Class information for:
Level 1: MCAD DEFICIENCY//MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY//UNIT MOL MED

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
3313 1937 28.5 76%


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 MCAD DEFICIENCY Author keyword 79 91% 2% 32
2 MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY Author keyword 55 77% 2% 37
3 UNIT MOL MED Address 43 39% 4% 85
4 ETHYLMALONIC ACID Author keyword 38 93% 1% 14
5 SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY Author keyword 35 89% 1% 16
6 3 METHYLCROTONYL COA CARBOXYLASE DEFICIENCY Author keyword 34 93% 1% 13
7 ETHYLMALONIC ACIDURIA Author keyword 31 92% 1% 12
8 VLCAD DEFICIENCY Author keyword 30 100% 1% 12
9 GLUTARIC ACIDURIA TYPE II Author keyword 29 88% 1% 14
10 LONG CHAIN 3 HYDROXYACYL COA DEHYDROGENASE DEFICIENCY Author keyword 27 92% 1% 11

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 MCAD DEFICIENCY 79 91% 2% 32 Search MCAD+DEFICIENCY Search MCAD+DEFICIENCY
2 MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY 55 77% 2% 37 Search MEDIUM+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY Search MEDIUM+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY
3 ETHYLMALONIC ACID 38 93% 1% 14 Search ETHYLMALONIC+ACID Search ETHYLMALONIC+ACID
4 SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY 35 89% 1% 16 Search SHORT+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY Search SHORT+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY
5 3 METHYLCROTONYL COA CARBOXYLASE DEFICIENCY 34 93% 1% 13 Search 3+METHYLCROTONYL+COA+CARBOXYLASE+DEFICIENCY Search 3+METHYLCROTONYL+COA+CARBOXYLASE+DEFICIENCY
6 ETHYLMALONIC ACIDURIA 31 92% 1% 12 Search ETHYLMALONIC+ACIDURIA Search ETHYLMALONIC+ACIDURIA
7 VLCAD DEFICIENCY 30 100% 1% 12 Search VLCAD+DEFICIENCY Search VLCAD+DEFICIENCY
8 GLUTARIC ACIDURIA TYPE II 29 88% 1% 14 Search GLUTARIC+ACIDURIA+TYPE+II Search GLUTARIC+ACIDURIA+TYPE+II
9 LONG CHAIN 3 HYDROXYACYL COA DEHYDROGENASE DEFICIENCY 27 92% 1% 11 Search LONG+CHAIN+3+HYDROXYACYL+COA+DEHYDROGENASE+DEFICIENCY Search LONG+CHAIN+3+HYDROXYACYL+COA+DEHYDROGENASE+DEFICIENCY
10 VLCAD 26 87% 1% 13 Search VLCAD Search VLCAD

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 MCAD DEFICIENCY 257 91% 6% 108
2 COENZYME A DEHYDROGENASE 115 46% 10% 186
3 COA DEHYDROGENASE DEFICIENCY 110 41% 11% 211
4 PREVALENT MUTATION 97 90% 2% 43
5 CHAIN 3 HYDROXYACYL COA DEHYDROGENASE 94 85% 3% 50
6 TRIFUNCTIONAL PROTEIN DEFICIENCY 77 84% 2% 42
7 ETHYLMALONIC ACIDURIA 73 85% 2% 39
8 G1528C MUTATION 70 89% 2% 32
9 ACIDEMIA TYPE II 50 73% 2% 38
10 3 HYDROXYDICARBOXYLIC ACIDURIA 50 88% 1% 23

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns 2003 279 109 56%
The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: An update 2006 59 33 97%
A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing 2005 82 33 67%
Newborn Screening: Need of the Hour in India 2015 1 25 28%
Fatty acid oxidation disorders 2002 155 86 55%
Mitochondrial Fatty-Acid Oxidation Disorders 2008 37 45 76%
NEUROPSYCHOLOGICAL OUTCOMES IN FATTY ACID OXIDATION DISORDERS: 85 CASES DETECTED BY NEWBORN SCREENING 2013 4 35 86%
Short-chain acyl-coenzyme A dehydrogenase deficiency 2008 28 42 86%
Regulation of mitochondrial fatty acid beta-oxidation in human: What can we learn from inborn fatty acid beta-oxidation deficiencies? 2014 3 86 64%
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship 2001 95 129 78%

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 UNIT MOL MED 43 39% 4.4% 85
2 UNITE ETUD MALAD METAB 6 71% 0.3% 5
3 KIMBERLY H COURTWRIGHT JOSEPH W SUMMERS ME 5 44% 0.4% 8
4 SERV BIOCHIM PEDIAT 4 33% 0.6% 11
5 BECKER 4 50% 0.3% 6
6 METAB DIS DETECT 3 57% 0.2% 4
7 INVEST BIOQUIM CLIN PATOL MOL 3 100% 0.2% 3
8 MED CLIN NEUROSCI FRAMLINGTON PL 3 100% 0.2% 3
9 BIOCHEM GENET MOL BIOL 3 40% 0.3% 6
10 NEWBORN SCREENING QUAL ASSURANCE PROGRAM 3 35% 0.4% 7

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000234340 ELECTRON TRANSFERRING FLAVOPROTEIN//ACYL COA DEHYDROGENASE//2 4 DIENOYL COA REDUCTASE
2 0.0000144948 L 2 HYDROXYGLUTARIC ACIDURIA//GLUTARIC ACIDURIA TYPE I//GLUTARIC ACIDURIA TYPE 1
3 0.0000127291 METHYLMALONIC ACIDEMIA//PROPIONIC ACIDEMIA//METHYLMALONIC ACIDURIA
4 0.0000113729 BETA KETOTHIOLASE DEFICIENCY//ACETOACETYL COA SYNTHETASE//3 HYDROXY 3 METHYLGLUTARIC ACIDURIA
5 0.0000113214 CARNITINE PALMITOYLTRANSFERASE//CARNITINE PALMITOYLTRANSFERASE DEFICIENCY//MITOCHONDRIAL HMG COA SYNTHASE
6 0.0000101991 NEWBORN SCREENING//CARRIER TESTING//CARRIER SCREENING
7 0.0000096676 DODECANEDIOIC ACID//AZELAIC ACID//DIETHYL SEBACATE
8 0.0000088034 CARNITINE//L CARNITINE//PROPIONYL L CARNITINE
9 0.0000078913 3 HYDROXYISOBUTYRATE DEHYDROGENASE//HIBCH//SERINE DEHYDROGENASE
10 0.0000060888 REYES SYNDROME//REYE SYNDROME//HLTH SCI MED COMPARAT MED