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Details
Link-It Detail - Human Phenotype - Abnormality of the cheeks
Debug Stats
  • ### Total Build Time: 20 ms 26.589 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 200 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
  • 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=2 ms Completed: 2 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 750 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.162 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 22.898 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cheeks HP:0004426
Parents (1)
img Abnormality of the midface HP:0000309
Children (2)
img Full cheeks HP:0000293
img Sunken cheeks HP:0009938
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the midface HP:0000309
Genes (43)

Species:
human : 43
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
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 RolledUp, OMIM ID: 614230
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanCLAM373073cerebellar atrophy with progressive microcephaly
img HP RolledUp, OMIM ID: 608027
HumanSH3PXD2B285590SH3 and PX domains 2B
img HP RolledUp, OMIM ID: 249420
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanWDR1957728WD repeat domain 19
img HP RolledUp, OMIM ID: 614378
img HP RolledUp, OMIM ID: 614376
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 605039
HumanGTF2IRD19569GTF2I repeat domain containing 1
img HP RolledUp, OMIM ID: 194050
HumanCRLF19244cytokine receptor-like factor 1
img HP RolledUp, OMIM ID: 601378
img HP RolledUp, OMIM ID: 272430
HumanMEHMO8422mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome
img HP RolledUp, OMIM ID: 300148
HumanTCF46925transcription factor 4
img HP RolledUp, OMIM ID: 610954
HumanTAZ6901tafazzin
img HP RolledUp, OMIM ID: 302060
HumanMAP2K25605mitogen-activated protein kinase kinase 2
img HP RolledUp, OMIM ID: 115150
HumanMAP2K15604mitogen-activated protein kinase kinase 1
img HP RolledUp, OMIM ID: 115150
HumanPIK3CA5290phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
img HP RolledUp, OMIM ID: 602501
HumanPCNT5116pericentrin
img HP RolledUp, OMIM ID: 210720
HumanPCCB5096propionyl CoA carboxylase, beta polypeptide
img HP RolledUp, OMIM ID: 232050
HumanPCCA5095propionyl CoA carboxylase, alpha polypeptide
img HP RolledUp, OMIM ID: 232000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004426Abnormality of the cheeks0self