Class information for:
Level 1: INCONTINENTIA PIGMENTI//HYPOMELANOSIS OF ITO//BLOCH SULZBERGER SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
14908 673 22.3 63%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
3008 2083 SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA

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 INCONTINENTIA PIGMENTI Author keyword 193 83% 16% 110
2 HYPOMELANOSIS OF ITO Author keyword 51 70% 6% 42
3 BLOCH SULZBERGER SYNDROME Author keyword 24 91% 1% 10
4 LINEAR AND WHORLED NEVOID HYPERMELANOSIS Author keyword 11 100% 1% 6
5 PROGRESSIVE MACULAR HYPOMELANOSIS Author keyword 11 100% 1% 6
6 NEMO GENE Author keyword 8 100% 1% 5
7 DIPLOID TRIPLOID MOSAICISM Author keyword 6 71% 1% 5
8 PITYRIASIS ALBA Author keyword 6 71% 1% 5
9 IKBKG GENE Author keyword 6 100% 1% 4
10 TRISOMY 13 MOSAICISM Author keyword 6 100% 1% 4

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 INCONTINENTIA PIGMENTI 193 83% 16% 110 Search INCONTINENTIA+PIGMENTI Search INCONTINENTIA+PIGMENTI
2 HYPOMELANOSIS OF ITO 51 70% 6% 42 Search HYPOMELANOSIS+OF+ITO Search HYPOMELANOSIS+OF+ITO
3 BLOCH SULZBERGER SYNDROME 24 91% 1% 10 Search BLOCH+SULZBERGER+SYNDROME Search BLOCH+SULZBERGER+SYNDROME
4 LINEAR AND WHORLED NEVOID HYPERMELANOSIS 11 100% 1% 6 Search LINEAR+AND+WHORLED+NEVOID+HYPERMELANOSIS Search LINEAR+AND+WHORLED+NEVOID+HYPERMELANOSIS
5 PROGRESSIVE MACULAR HYPOMELANOSIS 11 100% 1% 6 Search PROGRESSIVE+MACULAR+HYPOMELANOSIS Search PROGRESSIVE+MACULAR+HYPOMELANOSIS
6 NEMO GENE 8 100% 1% 5 Search NEMO+GENE Search NEMO+GENE
7 DIPLOID TRIPLOID MOSAICISM 6 71% 1% 5 Search DIPLOID+TRIPLOID+MOSAICISM Search DIPLOID+TRIPLOID+MOSAICISM
8 PITYRIASIS ALBA 6 71% 1% 5 Search PITYRIASIS+ALBA Search PITYRIASIS+ALBA
9 IKBKG GENE 6 100% 1% 4 Search IKBKG+GENE Search IKBKG+GENE
10 TRISOMY 13 MOSAICISM 6 100% 1% 4 Search TRISOMY+13+MOSAICISM Search TRISOMY+13+MOSAICISM

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 BLOCH SULZBERGER SYNDROME 101 84% 8% 56
2 INCONTINENTIA PIGMENTI ACHROMIANS 69 81% 6% 42
3 HYPOMELANOSIS 25 39% 7% 50
4 BLOCH SULZBERGER 15 82% 1% 9
5 ACHROMIANS 14 100% 1% 7
6 RETICULATE HYPERPIGMENTATION 11 69% 1% 9
7 FAMILIAL HYPOMELANOSIS 8 100% 1% 5
8 GENETIC MOSAICISM 8 41% 2% 15
9 MIXOPLOIDY 7 64% 1% 7
10 MOSAIC TRISOMY 13 6 71% 1% 5

Journals

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
Neurological findings in incontinentia pigmenti; a review 2012 14 51 73%
Systematic review of central nervous system anomalies in incontinentia pigmenti 2013 12 33 64%
Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature 2010 10 24 96%
Phenotypic Variability in Trisomy 13 Mosaicism: Two New Patients and Literature Review 2009 24 18 67%
Incontinentia pigmenti-ophthalmological observation of a series of cases and review of the literature 2011 10 29 79%
Progressive macular hypomelanosis - An overview 2007 22 9 100%
Incontinentia pigmenti (Bloch-Sulzberger syndrome): A systemic disorder 2007 22 86 87%
Dental and oral anomalies in incontinentia pigmenti: a systematic review 2013 6 25 64%
Ocular Anomalies in Incontinentia Pigmenti: Literature Review and Meta-Analysis 2010 5 15 87%
Male cases of incontinentia pigmenti: Case report and review 1998 39 21 81%

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 SERV NEURO CHIRURG 1 50% 0.1% 1
2 SETOR OFTALMOL 1 50% 0.1% 1
3 UNITE GENET HUMAINE MALAD INFECT 1 50% 0.1% 1
4 UR393 1 50% 0.1% 1
5 DERMATOVENEROL CLIN 1 29% 0.3% 2
6 U393UNITE RECH HANDIC S GENET ENFANT 1 29% 0.3% 2
7 ABT GENOMANALYSE 0 33% 0.1% 1
8 CHILD RADIOL 0 33% 0.1% 1
9 DERMATOL VENEOROL 0 33% 0.1% 1
10 IG I 0 33% 0.1% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000146579 ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS//EPIDERMAL NEVUS SYNDROME//OCULOCEREBROCUTANEOUS SYNDROME
2 0.0000122821 TRISOMY 18//TRISOMY 13//PATAU SYNDROME
3 0.0000117101 CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9
4 0.0000104252 AICARDI SYNDROME//GOLTZ SYNDROME//FOCAL DERMAL HYPOPLASIA
5 0.0000103398 DYSCHROMATOSIS SYMMETRICA HEREDITARIA//DOWLING DEGOS DISEASE//DSRAD GENE
6 0.0000085899 HUMAN GENET INFECT DIS//PEDIAT HEMATOL IMMUNOL UNIT//NECKER MED
7 0.0000076158 NEUROCUTANEOUS MELANOSIS//NEUROCUTANEOUS MELANOCYTOSIS//TWIN SPOTTING
8 0.0000054743 WAARDENBURG SYNDROME//WAARDENBURGS SYNDROME//KLEIN WAARDENBURG SYNDROME
9 0.0000053166 EDAR//HYPOHIDROTIC ECTODERMAL DYSPLASIA//ECTODERMAL DYSPLASIA
10 0.0000047047 SMITH LEMLI OPITZ SYNDROME//CHONDRODYSPLASIA PUNCTATA//7 DEHYDROCHOLESTEROL