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Details
Link-It Detail - Human Phenotype - Abnormality of the fontanelles and cranial sutures
Debug Stats
  • ### Total Build Time: 92 ms 31.829 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 225 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 4.615 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.092 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=63 ms Completed: 63 ms rowSize= 23.276 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.044 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the fontanelles and cranial sutures HP:0000235
Parents (1)
img Abnormality of the calvaria HP:0002683
Children (14)
img Wide cranial sutures HP:0010537
img Craniosynostosis HP:0001363
img Small fontanelles HP:0005486
img Abnormality of the anterior fontanelle HP:0000236
img Abnormality of the metopic suture HP:0005556
img Ridged cranial sutures HP:0010823
img Large fontanelles HP:0000239
img Delayed cranial suture closure HP:0000270
img Premature closure of fontanelles HP:0005458
img Sclerotic cranial sutures HP:0005441
img Premature posterior fontanelle closure HP:0005494
img Wormian bones HP:0002645
img Abnormality of cranial sutures HP:0011329
img Abnormality of fontanelles HP:0011328
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the calvaria HP:0002683
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the calvaria HP:0002683
Genes (191)

Species:
human : 191
Page Size
Current 25
  Page 1 of 8
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP TAS, OMIM ID: 614527
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP TAS, OMIM ID: 613509
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanPSS780904Potocki-Shaffer syndrome
img HP RolledUp, OMIM ID: 601224
HumanWTRS619509Wittwer syndrome
img HP TAS, OMIM ID: 300421
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
HumanLRSL406214Larsen-like syndrome
img HP RolledUp, OMIM ID: 608545
HumanIFITM5387733interferon induced transmembrane protein 5
img HP RolledUp, OMIM ID: 610967
HumanKIF7374654kinesin family member 7
img HP TAS, OMIM ID: 200990
HumanSH3PXD2B285590SH3 and PX domains 2B
img HP RolledUp, OMIM ID: 249420
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
img HP RolledUp, OMIM ID: 180860
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300215
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000235Abnormality of the fontanelles and cranial sutures0self