Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 32257 | 111 | 20.4 | 70% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 3033 | 1997 | HYPERTROPHIC OSTEOARTHROPATHY//SECKEL SYNDROME//PACHYDERMOPERIOSTOSIS |
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 | COHEN SYNDROME | Author keyword | 84 | 87% | 37% | 41 |
| 2 | COH1 | Author keyword | 18 | 89% | 7% | 8 |
| 3 | VPS13B | Author keyword | 11 | 100% | 5% | 6 |
| 4 | TRAPPED NEUTROPHIL SYNDROME | Author keyword | 3 | 100% | 3% | 3 |
| 5 | DISABLED PERSONS | Address | 2 | 67% | 2% | 2 |
| 6 | MENTAL HLTH SOCIAL WELF | Address | 2 | 67% | 2% | 2 |
| 7 | DISTINCTIVE FACIAL APPEARANCE | Author keyword | 1 | 50% | 1% | 1 |
| 8 | EYE DISEASES PATHOLOGY | Author keyword | 1 | 50% | 1% | 1 |
| 9 | GENET PAEDIAT ENDOCRINOL | Address | 1 | 50% | 1% | 1 |
| 10 | REFERENCE AFFECT GENET OPHTHALMOL | Address | 1 | 50% | 1% | 1 |
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 | COHEN SYNDROME | 84 | 87% | 37% | 41 | Search COHEN+SYNDROME | Search COHEN+SYNDROME |
| 2 | COH1 | 18 | 89% | 7% | 8 | Search COH1 | Search COH1 |
| 3 | VPS13B | 11 | 100% | 5% | 6 | Search VPS13B | Search VPS13B |
| 4 | TRAPPED NEUTROPHIL SYNDROME | 3 | 100% | 3% | 3 | Search TRAPPED+NEUTROPHIL+SYNDROME | Search TRAPPED+NEUTROPHIL+SYNDROME |
| 5 | DISTINCTIVE FACIAL APPEARANCE | 1 | 50% | 1% | 1 | Search DISTINCTIVE+FACIAL+APPEARANCE | Search DISTINCTIVE+FACIAL+APPEARANCE |
| 6 | EYE DISEASES PATHOLOGY | 1 | 50% | 1% | 1 | Search EYE+DISEASES+PATHOLOGY | Search EYE+DISEASES+PATHOLOGY |
| 7 | CHANGING PHENOTYPE | 0 | 33% | 1% | 1 | Search CHANGING+PHENOTYPE | Search CHANGING+PHENOTYPE |
| 8 | GYNAECOLOGY AND OBSTETRICS | 0 | 33% | 1% | 1 | Search GYNAECOLOGY+AND+OBSTETRICS | Search GYNAECOLOGY+AND+OBSTETRICS |
| 9 | CURLY HAIR | 0 | 25% | 1% | 1 | Search CURLY+HAIR | Search CURLY+HAIR |
| 10 | LOW VOLTAGE EEG | 0 | 25% | 1% | 1 | Search LOW+VOLTAGE+EEG | Search LOW+VOLTAGE+EEG |
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 | HOLMES WALTON SYNDROME | 15 | 88% | 6% | 7 |
| 2 | JEWISH TYPE | 3 | 100% | 3% | 3 |
| 3 | KEX2P | 2 | 50% | 3% | 3 |
| 4 | COHEN SYNDROME | 1 | 17% | 5% | 5 |
| 5 | WEIMARANER | 1 | 50% | 1% | 1 |
| 6 | FEMORAL NECK FRAGILITY | 0 | 13% | 1% | 1 |
| 7 | AUTOSOMAL RECESSIVE DISORDER | 0 | 11% | 1% | 1 |
| 8 | BORDER COLLIES | 0 | 11% | 1% | 1 |
| 9 | LENS OPACITY | 0 | 11% | 1% | 1 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| THE COHEN SYNDROME - REPORT OF 5 NEW CASES AND A REVIEW OF THE LITERATURE | 1982 | 22 | 2 | 100% |
| Obesity in Single Gene Disorders | 2010 | 5 | 150 | 8% |
| Finnish Disease Heritage I: characteristics, causes, background | 2003 | 67 | 26 | 4% |
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 | DISABLED PERSONS | 2 | 67% | 1.8% | 2 |
| 2 | MENTAL HLTH SOCIAL WELF | 2 | 67% | 1.8% | 2 |
| 3 | GENET PAEDIAT ENDOCRINOL | 1 | 50% | 0.9% | 1 |
| 4 | REFERENCE AFFECT GENET OPHTHALMOL | 1 | 50% | 0.9% | 1 |
| 5 | EYE DEV GENET GRP | 0 | 33% | 0.9% | 1 |
| 6 | GENET MOL PLATEAU TECH BIOL | 0 | 33% | 0.9% | 1 |
| 7 | REFERENCE AFFECT SENSORIELLES GENET | 0 | 33% | 0.9% | 1 |
| 8 | UO METAB DIS MED GENET | 0 | 33% | 0.9% | 1 |
| 9 | BGI EDUC | 0 | 20% | 0.9% | 1 |
| 10 | SERV GENET HUMAINE | 0 | 20% | 0.9% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000266895 | ASPM//MCPH1//WDR62 |
| 2 | 0.0000211108 | CUTIS VERTICIS GYRATA//CEREBRIFORM INTRADERMAL NEVUS//CEREBRIFORM INTRADERMAL NAEVUS |
| 3 | 0.0000144135 | ALSTROM SYNDROME//ALMS1//TUBBY |
| 4 | 0.0000141344 | MCLEOD SYNDROME//CHOREA ACANTHOCYTOSIS//NEUROACANTHOCYTOSIS |
| 5 | 0.0000097296 | ADAMS OLIVER SYNDROME//APLASIA CUTIS CONGENITA//SETLEIS SYNDROME |
| 6 | 0.0000094591 | SEVERE CONGENITAL NEUTROPENIA//HAX 1//CYCLIC NEUTROPENIA |
| 7 | 0.0000079522 | TRICHORHINOPHALANGEAL SYNDROME//TRPS1//TRICHO RHINO PHALANGEAL SYNDROME |
| 8 | 0.0000055767 | JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER |
| 9 | 0.0000055400 | SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM |
| 10 | 0.0000055136 | SCHIMKE IMMUNO OSSEOUS DYSPLASIA//SMARCAL1//SCHIMKE IMMUNOOSSEOUS DYSPLASIA |