Class information for:
Level 1: GLYCEROL KINASE DEFICIENCY//COMPLEX GLYCEROL KINASE DEFICIENCY//KOHLSCHUTTER TONZ SYNDROME

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
27999 177 26.2 60%



Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)



ID, lev.
above
Publications Label for level above
3239 1475 VDAC//MITOCHONDRIAL PORIN//VOLTAGE DEPENDENT ANION SELECTIVE CHANNEL

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 GLYCEROL KINASE DEFICIENCY Author keyword 41 87% 11% 20
2 COMPLEX GLYCEROL KINASE DEFICIENCY Author keyword 3 100% 2% 3
3 KOHLSCHUTTER TONZ SYNDROME Author keyword 3 100% 2% 3
4 HYPERGLYCEROLEMIA Author keyword 2 67% 1% 2
5 LANDESKLIN KINDER JUGENDHEILKUNDE Address 2 67% 1% 2
6 GLYCEROL KINASE Author keyword 2 15% 6% 11
7 PSEUDOHYPERTRIGLYCERIDEMIA Author keyword 1 100% 1% 2
8 XP21 Author keyword 1 50% 1% 2
9 XP21 CONTIGUOUS GENE DELETION SYNDROME Author keyword 1 100% 1% 2
10 ADRENAL HYPOPLASIA Author keyword 1 30% 2% 3

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 GLYCEROL KINASE DEFICIENCY 41 87% 11% 20 Search GLYCEROL+KINASE+DEFICIENCY Search GLYCEROL+KINASE+DEFICIENCY
2 COMPLEX GLYCEROL KINASE DEFICIENCY 3 100% 2% 3 Search COMPLEX+GLYCEROL+KINASE+DEFICIENCY Search COMPLEX+GLYCEROL+KINASE+DEFICIENCY
3 KOHLSCHUTTER TONZ SYNDROME 3 100% 2% 3 Search KOHLSCHUTTER+TONZ+SYNDROME Search KOHLSCHUTTER+TONZ+SYNDROME
4 HYPERGLYCEROLEMIA 2 67% 1% 2 Search HYPERGLYCEROLEMIA Search HYPERGLYCEROLEMIA
5 GLYCEROL KINASE 2 15% 6% 11 Search GLYCEROL+KINASE Search GLYCEROL+KINASE
6 PSEUDOHYPERTRIGLYCERIDEMIA 1 100% 1% 2 Search PSEUDOHYPERTRIGLYCERIDEMIA Search PSEUDOHYPERTRIGLYCERIDEMIA
7 XP21 1 50% 1% 2 Search XP21 Search XP21
8 XP21 CONTIGUOUS GENE DELETION SYNDROME 1 100% 1% 2 Search XP21+CONTIGUOUS+GENE+DELETION+SYNDROME Search XP21+CONTIGUOUS+GENE+DELETION+SYNDROME
9 ADRENAL HYPOPLASIA 1 30% 2% 3 Search ADRENAL+HYPOPLASIA Search ADRENAL+HYPOPLASIA
10 ALUY INSERTION 1 50% 1% 1 Search ALUY+INSERTION Search ALUY+INSERTION

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 CONGENITAL ADRENAL HYPOPLASIA 13 48% 11% 20
2 YELLOW TEETH 11 100% 3% 6
3 DXS67 B24 6 80% 2% 4
4 HYPERGLYCEROLEMIA 6 71% 3% 5
5 RECEPTOR TRANSLOCATION PROMOTER 4 75% 2% 3
6 STIMULATED FACTOR 4 75% 2% 3
7 GLYCEROL KINASE DEFICIENCY 3 21% 8% 15
8 GLYCEROL KINASE GENE 3 60% 2% 3
9 XP21 2 17% 6% 11
10 PSEUDO HYPERTRIGLYCERIDEMIA 1 100% 1% 2

Journals

Reviews



Title Publ. year Cit. Active references % act. ref.
to same field
Identifying pseudohypertriglyceridemia in clinical practice 2014 0 40 50%
Conserved family of glycerol kinase loci in Drosophila melanogaster 2006 12 83 22%
Single-gene disorders: What role could moonlighting enzymes play? 2005 102 108 7%
Consequences of complexity within biological networks: Robustness and health, or vulnerability and disease 2001 70 11 9%

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 LANDESKLIN KINDER JUGENDHEILKUNDE 2 67% 1.1% 2
2 MOLEC GENET GRP 1 50% 0.6% 1
3 PATHOL MUSCULAIRE 1 50% 0.6% 1
4 SE THAMES REG GENET 1 50% 0.6% 1
5 UNIDAD RIESGO CARDIOVASC 1 50% 0.6% 1
6 EXPLORAT READ TAT ANOMALIES METAB MUSCUL 0 33% 0.6% 1
7 TORAT OPERAT DENT 0 33% 0.6% 1
8 MED GENET METAB DIS 0 25% 0.6% 1
9 REG NEONATAL SCREENING 0 25% 0.6% 1
10 CLIN CHEM 2P8 0 20% 0.6% 1

Related classes at same level (level 1)



Rank Relatedness score Related classes
1 0.0000251457 ADRENAL HYPOPLASIA CONGENITA//DAX 1//STEROIDOGENIC FACTOR 1
2 0.0000166536 DYSTROPHIN//BECKER MUSCULAR DYSTROPHY//DUCHENNE MUSCULAR DYSTROPHY
3 0.0000090153 FRUCTOSE 1 6 BISPHOSPHATASE//FBPASE//MUSCLE FBPASE
4 0.0000086379 VDAC//MITOCHONDRIAL PORIN//VOLTAGE DEPENDENT ANION SELECTIVE CHANNEL
5 0.0000064783 TI TPYP REAGENT//GPO//GLYCEROL 3 PHOSPHATE OXIDASE
6 0.0000060822 X LINKED MENTAL RETARDATION//XLMR//PQBP1
7 0.0000046573 BETA KETOTHIOLASE DEFICIENCY//ACETOACETYL COA SYNTHETASE//3 HYDROXY 3 METHYLGLUTARIC ACIDURIA
8 0.0000041974 GLYCEROL PHOSPHATE DEHYDROGENASE//ALPHA GLYCEROL 3 PHOSPHATE DEHYDROGENASE//ANXIETY DEPRESSIVE SYNDROME
9 0.0000041003 TAIL BIOPSY//CHICKEN BETA ACTIN PROMOTER//ANALYTICAL PITFALLS
10 0.0000036204 CHROMOSOME SORTING//FLOW KARYOTYPE//CHROMOSOME ISOLATION