Class information for:
Level 1: ORNITHINE TRANSCARBAMYLASE DEFICIENCY//SLC25A13//CITRIN DEFICIENCY

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
4975 1625 25.0 64%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1850 5585 ARGINASE//ORNITHINE TRANSCARBAMYLASE DEFICIENCY//SLC25A13

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 ORNITHINE TRANSCARBAMYLASE DEFICIENCY Author keyword 146 80% 6% 90
2 SLC25A13 Author keyword 112 97% 2% 32
3 CITRIN DEFICIENCY Author keyword 98 100% 2% 29
4 CITRULLINEMIA Author keyword 71 75% 3% 51
5 HYPERAMMONEMIA Author keyword 68 30% 12% 193
6 MOL METAB BIOCHEM GENET Address 67 76% 3% 47
7 UREA CYCLE DISORDERS Author keyword 59 67% 3% 53
8 CITRIN Author keyword 47 84% 2% 26
9 ADULT ONSET TYPE II CITRULLINEMIA Author keyword 44 100% 1% 16
10 ORNITHINE TRANSCARBAMYLASE Author keyword 36 57% 3% 43

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 ORNITHINE TRANSCARBAMYLASE DEFICIENCY 146 80% 6% 90 Search ORNITHINE+TRANSCARBAMYLASE+DEFICIENCY Search ORNITHINE+TRANSCARBAMYLASE+DEFICIENCY
2 SLC25A13 112 97% 2% 32 Search SLC25A13 Search SLC25A13
3 CITRIN DEFICIENCY 98 100% 2% 29 Search CITRIN+DEFICIENCY Search CITRIN+DEFICIENCY
4 CITRULLINEMIA 71 75% 3% 51 Search CITRULLINEMIA Search CITRULLINEMIA
5 HYPERAMMONEMIA 68 30% 12% 193 Search HYPERAMMONEMIA Search HYPERAMMONEMIA
6 UREA CYCLE DISORDERS 59 67% 3% 53 Search UREA+CYCLE+DISORDERS Search UREA+CYCLE+DISORDERS
7 CITRIN 47 84% 2% 26 Search CITRIN Search CITRIN
8 ADULT ONSET TYPE II CITRULLINEMIA 44 100% 1% 16 Search ADULT+ONSET+TYPE+II+CITRULLINEMIA Search ADULT+ONSET+TYPE+II+CITRULLINEMIA
9 ORNITHINE TRANSCARBAMYLASE 36 57% 3% 43 Search ORNITHINE+TRANSCARBAMYLASE Search ORNITHINE+TRANSCARBAMYLASE
10 UREA CYCLE 35 33% 5% 86 Search UREA+CYCLE Search UREA+CYCLE

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 UREA CYCLE DISORDERS 135 60% 9% 149
2 II CITRULLINEMIA 117 79% 5% 75
3 ORNITHINE TRANSCARBAMYLASE DEFICIENCY 105 51% 9% 146
4 CLASSICAL CITRULLINEMIA 102 100% 2% 30
5 CARBAMOYL TRANSFERASE DEFICIENCY 73 96% 1% 23
6 NICCD 69 96% 1% 22
7 UREA CYCLE ENZYMOPATHIES 41 90% 1% 18
8 CARBAMOYLTRANSFERASE DEFICIENCY 41 87% 1% 20
9 ALTERNATIVE PATHWAY THERAPY 38 89% 1% 17
10 OTC DEFICIENCY 35 89% 1% 16

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Suggested guidelines for the diagnosis and management of urea cycle disorders 2012 40 224 68%
Molecular genetics of citrullinemia types I and II 2014 3 92 93%
Hyperammonemia in review: pathophysiology, diagnosis, and treatment 2012 18 90 63%
Diagnosis and treatment of urea cycle disorder in Japan 2014 2 20 90%
Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD) 2002 86 58 76%
Clinical practice The management of hyperammonemia 2011 17 57 61%
Ammonium metabolism in humans 2012 31 135 27%
Ammonia toxicity and its prevention in inherited defects of the urea cycle 2009 26 98 59%
Contrasting features of urea cycle disorders in human patients and knockout mouse models 2008 25 78 71%
Recurrent Encephalopathy: NAGS (N-Acetylglutamate Synthase) Deficiency in Adults 2013 3 45 93%

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 MOL METAB BIOCHEM GENET 67 76% 2.9% 47
2 UNITAT METABOLOPATIES 3 60% 0.2% 3
3 HUMAN GENET MED GENET 2 44% 0.2% 4
4 MAINE PEDIAT SPECIALTY GRP 2 67% 0.1% 2
5 UNIV KLIN CHEM 2 67% 0.1% 2
6 MED KENNEDY 1 50% 0.1% 2
7 METAB DIS CLIN GENET UNIT 1 100% 0.1% 2
8 UNIV CLIN CHEM 1 19% 0.3% 5
9 INTEGRAT PHYSIOL VET SCI 1 19% 0.3% 5
10 REFERENCE MALADIES HEREDITAI METAB 1 40% 0.1% 2

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000090068 NONKETOTIC HYPERGLYCINEMIA//NON KETOTIC HYPERGLYCINEMIA//GLYCINE N ACYLTRANSFERASE
2 0.0000084733 PREGNANCY DISTURBED//BRAIN NEWBORN//CSIC BIOL MOLEC BIOL MOLEC
3 0.0000079673 METHYLMALONIC ACIDEMIA//PROPIONIC ACIDEMIA//METHYLMALONIC ACIDURIA
4 0.0000078510 ARGINASE//NOR NOHA//ARGINASE II
5 0.0000076907 CITRULLINE//HUBEI ANIM NUTR FEED SCI//HUNAN ENGN ANIM POULTRY SCI
6 0.0000071592 METABOLIC ZONATION//BIVASCULAR LIVER PERFUSION//CARBAMOYLPHOSPHATE SYNTHETASE I
7 0.0000071557 DIHYDROOROTASE//CARBAMOYL PHOSPHATE SYNTHETASE//ASPARTATE CARBAMOYLTRANSFERASE
8 0.0000067571 BLEOMYCIN AMPLIFICATION//PHENYLACETATE//ANTINEOPLASTON AS2 1
9 0.0000066865 HEPATIC ENCEPHALOPATHY//MINIMAL HEPATIC ENCEPHALOPATHY//METABOLIC BRAIN DISEASE
10 0.0000055624 GYRATE ATROPHY//GYRATE ATROPHY OF THE CHOROID AND RETINA//ORNITHINE AMINOTRANSFERASE