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Details
Link-It Detail - Human Phenotype - Abnormality of the palate
Debug Stats
  • ### Total Build Time: 37 ms 29.454 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 227 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= 451 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 3.277 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 22.989 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.020 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of the palate HP:0000174
Definition (1)
Any abnormality of the `palate` (FMA:54549), i.e., of roof of the mouth).
Parents (1)
img Abnormality of the oral cavity HP:0000163
Children (10)
img Oral cleft HP:0000202
img Palate telangiectasia HP:0002707
img Abnormality of the hard palate HP:0100737
img Prominent palatine ridges HP:0010291
img Prominent median palatal raphe HP:0002708
img Short hard palate HP:0010290
img Narrow palate HP:0000189
img High palate HP:0000218
img Abnormality of the soft palate HP:0100736
img Palate fistula HP:0010294
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the oral cavity HP:0000163
Genes (488)

Species:
human : 488
Page Size
Current 25
  Page 1 of 20
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP TAS, OMIM ID: 166750
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP TAS, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
img HP RolledUp, OMIM ID: 612530
HumanDUP17Q21.31100529226
img HP TAS, OMIM ID: 613533
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP TAS, OMIM ID: 613457
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP TAS, OMIM ID: 613406
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanDUP17P13.3100379203
img HP TAS, OMIM ID: 613215
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanPRBNS100301572Pierre Robin syndrome
img HP RolledUp, OMIM ID: 261800
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000174Abnormality of the palate0self