Class information for:
Level 2: HYPERTROPHIC OSTEOARTHROPATHY//SECKEL SYNDROME//PACHYDERMOPERIOSTOSIS

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
3033 1997 22.5 60%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)


ID, lev.
above		 Publications Label for level above
544 16108 ALOPECIA AREATA//ANDROGENETIC ALOPECIA//ALOPECIA

Classes in level below (level 1)


ID, lev. below Publications Label for level below
15123 660 HYPERTROPHIC OSTEOARTHROPATHY//PACHYDERMOPERIOSTOSIS//HYPERTROPHIC OSTEOPATHY
19824 424 ACCESSORY SCROTUM//CONGENITAL HYPERTRICHOSIS//CANTU SYNDROME
20252 406 ASPM//MCPH1//WDR62
22416 325 SECKEL SYNDROME//FLOATING HARBOR SYNDROME//MOPD II
32257 111 COHEN SYNDROME//COH1//VPS13B
34443 71 CUTIS VERTICIS GYRATA//CEREBRIFORM INTRADERMAL NEVUS//CEREBRIFORM INTRADERMAL NAEVUS

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 HYPERTROPHIC OSTEOARTHROPATHY Author keyword 134 80% 4% 82
2 SECKEL SYNDROME Author keyword 101 84% 3% 56
3 PACHYDERMOPERIOSTOSIS Author keyword 96 83% 3% 54
4 FLOATING HARBOR SYNDROME Author keyword 91 94% 2% 32
5 COHEN SYNDROME Author keyword 84 87% 2% 41
6 ASPM Author keyword 44 85% 1% 23
7 CUTIS VERTICIS GYRATA Author keyword 41 85% 1% 22
8 HYPERTROPHIC OSTEOPATHY Author keyword 40 77% 1% 27
9 DIGITAL CLUBBING Author keyword 37 75% 1% 27
10 PRIMARY HYPERTROPHIC OSTEOARTHROPATHY Author keyword 34 79% 1% 22

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 HYPERTROPHIC OSTEOARTHROPATHY 134 80% 4% 82 Search HYPERTROPHIC+OSTEOARTHROPATHY Search HYPERTROPHIC+OSTEOARTHROPATHY
2 SECKEL SYNDROME 101 84% 3% 56 Search SECKEL+SYNDROME Search SECKEL+SYNDROME
3 PACHYDERMOPERIOSTOSIS 96 83% 3% 54 Search PACHYDERMOPERIOSTOSIS Search PACHYDERMOPERIOSTOSIS
4 FLOATING HARBOR SYNDROME 91 94% 2% 32 Search FLOATING+HARBOR+SYNDROME Search FLOATING+HARBOR+SYNDROME
5 COHEN SYNDROME 84 87% 2% 41 Search COHEN+SYNDROME Search COHEN+SYNDROME
6 ASPM 44 85% 1% 23 Search ASPM Search ASPM
7 CUTIS VERTICIS GYRATA 41 85% 1% 22 Search CUTIS+VERTICIS+GYRATA Search CUTIS+VERTICIS+GYRATA
8 HYPERTROPHIC OSTEOPATHY 40 77% 1% 27 Search HYPERTROPHIC+OSTEOPATHY Search HYPERTROPHIC+OSTEOPATHY
9 DIGITAL CLUBBING 37 75% 1% 27 Search DIGITAL+CLUBBING Search DIGITAL+CLUBBING
10 PRIMARY HYPERTROPHIC OSTEOARTHROPATHY 34 79% 1% 22 Search PRIMARY+HYPERTROPHIC+OSTEOARTHROPATHY Search PRIMARY+HYPERTROPHIC+OSTEOARTHROPATHY

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 PACHYDERMOPERIOSTOSIS 80 80% 2% 49
2 PULMONARY OSTEOARTHROPATHY 77 89% 2% 34
3 SECKEL SYNDROME 40 46% 3% 66
4 HYPERTROPHIC OSTEOARTHROPATHY 36 48% 3% 54
5 PRIMARY HYPERTROPHIC OSTEOARTHROPATHY 35 67% 2% 32
6 CONGENITAL HYPERTRICHOSIS 32 85% 1% 17
7 ASPM GENE 32 78% 1% 21
8 SMOOTH MUSCLE HAMARTOMA 29 71% 1% 24
9 BRIT1 MCPH1 29 88% 1% 14
10 PRIMORDIAL DWARFISM 28 57% 2% 34

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Molecular genetics of human primary microcephaly: an overview 2015 1 85 66%
Primary microcephaly: do all roads lead to Rome? 2009 140 69 43%
Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum 2011 51 103 76%
Emerging roles of MCPH1: Expedition from primary microcephaly to cancer 2014 5 76 68%
Autosomal recessive primary microcephaly (MCPH): A review of clinical, molecular, and evolutionary findings 2005 167 70 49%
What primary microcephaly can tell us about brain growth 2006 83 63 56%
Many roads lead to primary autosomal recessive microcephaly 2010 53 108 52%
Hypertrophic pulmonary osteoarthropathy (HPOA) (Pierre Marie-Bamberger syndrome): two cases presenting as acute inflammatory arthritis. Description and review of the literature 2007 19 7 100%
Periostitis and Hypertrophic Pulmonary Osteoarthropathy: Report of 2 Cases and Review of the Literature 2009 23 71 83%
Pachydermoperiostosis: an update 2005 60 40 78%

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 HUMAN DNA DAMAGE PONSE DISORDERS GRP 7 50% 0.5% 10
2 DISABLED PERSONS 2 67% 0.1% 2
3 GENET HUMANA CLIN ASESORAMIENTO GENET 2 67% 0.1% 2
4 HGU 2 67% 0.1% 2
5 MENTAL HLTH SOCIAL WELF 2 67% 0.1% 2
6 DOUBLE STRAND BREAK REPAIR 1 100% 0.1% 2
7 REFERENCE ANOMALIES DEV SYNDROMES MALFORMAT 1 14% 0.4% 8
8 MARITIME MED GENET SERV 1 20% 0.3% 5
9 ORODENTAL GENET 1 30% 0.2% 3
10 HUMAN GENET 836 1 40% 0.1% 2

Related classes at same level (level 2)


Rank Relatedness score Related classes
1 0.0000014899 KABUKI SYNDROME//KABUKI MAKE UP SYNDROME//TRICHORHINOPHALANGEAL SYNDROME
2 0.0000011073 RHOMBENCEPHALOSYNAPSIS//PONTOCEREBELLAR HYPOPLASIA//ARTHROGRYPOSIS
3 0.0000010349 FIBRILLARY GLOMERULONEPHRITIS//NAIL PATELLA SYNDROME//YELLOW NAIL SYNDROME
4 0.0000009563 POROKERATOSIS//DYSCHROMATOSIS SYMMETRICA HEREDITARIA//ACANTHOSIS NIGRICANS
5 0.0000007798 KINETOCHORE//MITOSIS//CENTROSOME
6 0.0000006747 REELIN//DAB1//VLDLR
7 0.0000005755 RETT SYNDROME//MECP2//MECP2 GENE
8 0.0000005583 ALOPECIA AREATA//ANDROGENETIC ALOPECIA//ALOPECIA
9 0.0000005430 SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA
10 0.0000005133 FANCONI ANEMIA//ATAXIA TELANGIECTASIA//WERNER SYNDROME