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Details
Link-It Detail - Human Phenotype - Abnormal palmar dermatoglyphics
Debug Stats
  • ### Total Build Time: 41 ms 34.186 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 280 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= 1.072 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.713 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 5.788 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=24 ms Completed: 24 ms rowSize= 22.968 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal palmar dermatoglyphics HP:0001018
Definition (1)
An abnormality of the dermatoglyphs, i.e., an abnormality of the patterns of ridges of the `skin of palm of hand` (FMA:38301).
Parents (3)
img Abnormality of the palm HP:0100871
img Abnormal dermatoglyphics HP:0007477
img Abnormality of the hand HP:0001155
Children (8)
img Prominent interdigital folds HP:0006189
img Dermatoglyphic ridges abnormal HP:0005689
img High axial triradius HP:0001042
img Increased dermatoglyphic whorls HP:0005875
img Complex palmar dermatoglyphic pattern HP:0007602
img Abnormal palmar dermal ridges HP:0007608
img Abnormality of the palmar creases HP:0010490
img Dermatoglyphic variants HP:0005882
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the palm HP:0100871
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the palm HP:0100871
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormal dermatoglyphics HP:0007477
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal dermatoglyphics HP:0007477
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the hand HP:0001155
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the hand HP:0001155
Genes (127)

Species:
human : 127
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanJAWAD100192306Microcephaly with digital anomalies
img HP RolledUp, OMIM ID: 251255
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanPSS780904Potocki-Shaffer syndrome
img HP RolledUp, OMIM ID: 601224
HumanWTRS619509Wittwer syndrome
img HP RolledUp, OMIM ID: 300421
HumanMSSD619407syndactyly, mesoaxial synostotic, with phalangeal reduction
img HP RolledUp, OMIM ID: 609432
HumanCVMRF494028cubitus valgus with mental retardation and unusual facies
img HP RolledUp, OMIM ID: 300471
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
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
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001018Abnormal palmar dermatoglyphics0self