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Details
Link-It Detail - Human Phenotype - Abnormality of the calvaria
Debug Stats
  • ### Total Build Time: 65 ms 23.630 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=1 ms Completed: 1 ms rowSize= 291 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 2.697 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.086 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 16.765 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the calvaria HP:0002683
Definition (1)
Abnormality of the `calvaria` (FMA:52800), which is the roof of the skull formed by the frontal bone, parietal bones, and occipital bone.
Parents (1)
img Abnormality of the skull HP:0000929
Children (8)
img Dense calvaria HP:0000250
img Cranial hyperostosis HP:0004437
img Abnormality of the fontanelles and cranial sutures HP:0000235
img Abnormality of calvarial morphology HP:0002648
img Abnormality of the parietal bone HP:0002696
img Thin calvarium HP:0010539
img Decreased calvarial ossification HP:0005474
img Thickened calvaria HP:0002684
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the skull HP:0000929
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the skull HP:0000929
Genes (496)

Species:
human : 496
Page Size
Current 25
  Page 1 of 20
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanCATMANS100862706Catel-Manzke syndrome
HumanCPBHM100820762Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
HumanDEL17P13.1100653374
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
HumanTRIP4Q32.1Q32.2100529228
HumanFWS100529224Forsythe-Wakeling syndrome
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL16P12.1P11.2100526742
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
HumanDEL17Q23.1Q23.2100415941
HumanDUP17P13.3100379203
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002683Abnormality of the calvaria0self