Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
18404 | 488 | 18.8 | 60% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1088 | 9330 | STURGE WEBER SYNDROME//INFANTILE HEMANGIOMA//HEMANGIOMA |
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 | ADAMS OLIVER SYNDROME | Author keyword | 120 | 91% | 10% | 50 |
2 | APLASIA CUTIS CONGENITA | Author keyword | 82 | 68% | 15% | 73 |
3 | SETLEIS SYNDROME | Author keyword | 23 | 100% | 2% | 10 |
4 | CUTIS MARMORATA TELANGIECTATICA CONGENITA | Author keyword | 21 | 71% | 3% | 17 |
5 | CUTIS MARMORATA TELANGIECTATICA | Author keyword | 20 | 100% | 2% | 9 |
6 | CUTIS APLASIA | Author keyword | 14 | 60% | 3% | 15 |
7 | CUTIS MARMORATA | Author keyword | 13 | 61% | 3% | 14 |
8 | APLASIA CUTIS CONGENITAL | Author keyword | 9 | 64% | 2% | 9 |
9 | FOCAL FACIAL DERMAL DYSPLASIA | Author keyword | 9 | 83% | 1% | 5 |
10 | MACROCEPHALY CUTIS MARMORATA TELANGIECTATICA CONGENITA | Author keyword | 8 | 100% | 1% | 5 |
Web of Science journal categories |
Author Key Words |
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 | DISTAL LIMB ANOMALIES | 34 | 93% | 3% | 13 |
2 | APLASIA CUTIS CONGENITA | 24 | 37% | 10% | 51 |
3 | CONGENITAL SCALP DEFECTS | 23 | 100% | 2% | 10 |
4 | ADAMS OLIVER SYNDROME | 20 | 48% | 6% | 31 |
5 | FORCEPS MARKS SYNDROME | 20 | 100% | 2% | 9 |
6 | CUTIS MARMORATA | 19 | 63% | 4% | 19 |
7 | MARMORATA TELANGIECTATICA CONGENITA | 17 | 42% | 6% | 31 |
8 | FACIAL DERMAL DYSPLASIA | 14 | 100% | 1% | 7 |
9 | DISTINCTIVE OVERGROWTH SYNDROME | 11 | 100% | 1% | 6 |
10 | TELEANGIECTATICA CONGENITA | 11 | 100% | 1% | 6 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
The Spectra of Clinical Phenotypes in Aplasia Cutis Congenita and Terminal Transverse Limb Defects | 2009 | 26 | 55 | 91% |
Macrocephaly-Capillary Malformation: Analysis of 13 Patients and Review of the Diagnostic Criteria | 2010 | 14 | 24 | 79% |
Macrocephaly-capillary malformation syndrome: Description of a case and review of clinical diagnostic criteria | 2012 | 7 | 9 | 89% |
Aplasia Cutis Congenita: Review of 29 Cases and Proposal of a Therapeutic Strategy | 2013 | 4 | 3 | 100% |
Mri and neurological findings in Macrocephaly-Cutis Marmorata Telangiectatica Congenita syndrome: Report of ten cases and review of the literature | 2005 | 16 | 10 | 90% |
CUTIS MARMORATA TELANGIECTATICA CONGENITA - REPORT OF 22 CASES | 1989 | 48 | 5 | 100% |
Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification | 2011 | 5 | 21 | 90% |
Type V Aplasia Cutis Congenita: Case Report, Review of the Literature, and Proposed Treatment Algorithm | 2013 | 1 | 20 | 80% |
CONGENITAL SCALP DEFECTS WITH DISTAL LIMB ANOMALIES (ADAMS-OLIVER SYNDROME) - REPORT OF 10 CASES AND REVIEW OF THE LITERATURE | 1988 | 60 | 7 | 86% |
Cutis marmorata telangiectatica congenita in a preterm newborn - Case report and literature review | 2012 | 0 | 13 | 100% |
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 | KLIN POLIKLIN DERMATOL BIEDERSTEIN | 1 | 50% | 0.2% | 1 |
2 | MED GENET PEDIAT CARDIOL | 1 | 50% | 0.2% | 1 |
3 | PEDIAT HEPATOL LIVER TRANSPLANTAT UNIT | 1 | 50% | 0.2% | 1 |
4 | PEDIAT IMAGERIE FOETALE | 1 | 50% | 0.2% | 1 |
5 | PL 3 | 1 | 50% | 0.2% | 1 |
6 | RAYMOND C PHILIP EDUC UNIT | 1 | 50% | 0.2% | 1 |
7 | REFERENCE MALFORMAT CRANIO MAXILLO IALES R | 1 | 50% | 0.2% | 1 |
8 | SC NEONATOL TER IA INTENS NEONATALE | 1 | 50% | 0.2% | 1 |
9 | DOERNBECHER NEONATAL CARE | 0 | 33% | 0.2% | 1 |
10 | ESTUDIO CO ORAT LATINOAMER MALFORMAC CONGENITAS | 0 | 33% | 0.2% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000097296 | COHEN SYNDROME//COH1//VPS13B |
2 | 0.0000096883 | ANGIOMA SERPIGINOSUM//HEREDITARY BENIGN TELANGIECTASIA//GENERALIZED ESSENTIAL TELANGIECTASIA |
3 | 0.0000088312 | AMNIOTIC BAND SYNDROME//LIMB BODY WALL COMPLEX//BODY STALK ANOMALY |
4 | 0.0000075910 | KLIPPEL TRENAUNAY SYNDROME//KLIPPEL TRENAUNAY WEBER SYNDROME//RASA1 |
5 | 0.0000065553 | PROTEUS SYNDROME//MACRODACTYLY//MACRODYSTROPHIA LIPOMATOSA |
6 | 0.0000061224 | WIEDEMANN RAUTENSTRAUCH SYNDROME//NEONATAL PROGEROID SYNDROME//HALLERMANN STREIFF SYNDROME |
7 | 0.0000058872 | ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS//EPIDERMAL NEVUS SYNDROME//OCULOCEREBROCUTANEOUS SYNDROME |
8 | 0.0000052371 | EDAR//HYPOHIDROTIC ECTODERMAL DYSPLASIA//ECTODERMAL DYSPLASIA |
9 | 0.0000052004 | AICARDI SYNDROME//GOLTZ SYNDROME//FOCAL DERMAL HYPOPLASIA |
10 | 0.0000049198 | SNEDDONS SYNDROME//SNEDDON SYNDROME//LIVEDOID VASCULOPATHY |