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Details
Link-It Detail - Human Phenotype - Abnormality of cranial sutures
Debug Stats
  • ### Total Build Time: 25 ms 27.279 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 205 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 302 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 471 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.995 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.137 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 20.023 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.024 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of cranial sutures HP:0011329
Definition (1)
Any anomaly of a cranial suture, that is one of the six membrane-covered openings in the incompletely ossified skull of the fetus or newborn infant.
Parents (1)
img Abnormality of the fontanelles and cranial sutures HP:0000235
Children (9)
img Wide cranial sutures HP:0010537
img Craniosynostosis HP:0001363
img Abnormality of the metopic suture HP:0005556
img Widely patent sagittal suture HP:0005476
img Ridged cranial sutures HP:0010823
img Delayed cranial suture closure HP:0000270
img Sclerotic cranial sutures HP:0005441
img Wormian bones HP:0002645
img Widely patent coronal suture HP:0005442
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the fontanelles and cranial sutures HP:0000235
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the fontanelles and cranial sutures HP:0000235
Genes (139)

Species:
human : 139
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanDEL3PTERP251006533853p- syndrome
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanDEL2P16.1-P15100240740
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanDEL17Q21.31791085
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanPSS780904Potocki-Shaffer syndrome
img HP RolledUp, OMIM ID: 601224
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
HumanIFITM5387733interferon induced transmembrane protein 5
img HP RolledUp, OMIM ID: 610967
HumanSH3PXD2B285590SH3 and PX domains 2B
img HP RolledUp, OMIM ID: 249420
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 180860
HumanASXL1171023additional sex combs like 1 (Drosophila)
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img HP RolledUp, OMIM ID: 268300
img HP RolledUp, OMIM ID: 269000
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
HumanRSS140821Russell Silver syndrome
img HP RolledUp, OMIM ID: 180860
HumanAMER1139285APC membrane recruitment protein 1
HumanSP7121340Sp7 transcription factor
img HP RolledUp, OMIM ID: 613849
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
HumanDBA2114086Diamond-Blackfan anemia 2
img HP RolledUp, OMIM ID: 105650
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011329Abnormality of cranial sutures0self