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Details
Link-It Detail - Human Phenotype - Abnormal dermatoglyphics
Debug Stats
  • ### Total Build Time: 32 ms 26.862 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 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=3 ms Completed: 3 ms rowSize= 775 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.717 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.089 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 20.693 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal dermatoglyphics HP:0007477
Definition (1)
An abnormality of dermatoglyphs (fingerprints), which are present on fingers, palms, toes, and soles.
Parents (2)
img Regional abnormality of skin HP:0011356
img Abnormality of the skin HP:0000951
Children (5)
img Abnormal palmar dermatoglyphics HP:0001018
img Adermatoglyphia HP:0007455
img Abnormal plantar dermatoglyphics HP:0010506
img Palmoplantar cutis gyrata HP:0007469
img Interdigital loops HP:0100888
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Regional abnormality of skin HP:0011356
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the skin HP:0000951
Genes (151)

Species:
human : 151
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCATMANS100862706Catel-Manzke syndrome
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
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP TAS, OMIM ID: 613884
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
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanJAWAD100192306Microcephaly with digital anomalies
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
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
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP TAS, OMIM ID: 300519
HumanCVMRF494028cubitus valgus with mental retardation and unusual facies
img HP RolledUp, OMIM ID: 300471
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP TAS, OMIM ID: 300519
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0007477Abnormal dermatoglyphics0self