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Details
Link-It Detail - Human Phenotype - Abnormality of the fingernails
Debug Stats
  • ### Total Build Time: 39 ms 35.078 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 205 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= 768 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.017 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 6.704 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 23.238 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the fingernails HP:0001231
Parents (2)
img Abnormality of finger HP:0001167
img Abnormality of the nail HP:0001597
Children (9)
img Ridged fingernail HP:0008402
img Aplastic/hypoplastic fingernail HP:0008384
img Nail bed telangiectasia HP:0001232
img Hyperconvex fingernails HP:0001812
img Onycholysis of distal fingernails HP:0008400
img Dystrophic fingernails HP:0008391
img Recurrent loss of toenails and fingernails HP:0008390
img Fingernail dysplasia HP:0100798
img Short and broad fingernails HP:0008406
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the nail HP:0001597
Genes (123)

Species:
human : 123
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
HumanECTD5101101769Ectodermal dysplasia 5, hair/nail type
img HP RolledUp, OMIM ID: 614927
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
HumanNDNC9100682325Nail disorder, nonsyndromic congenital, 9
img HP RolledUp, OMIM ID: 614149
HumanDEL19Q13.11100306978
img HP TAS, OMIM ID: 613026
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP TAS, OMIM ID: 158170
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP TAS, OMIM ID: 601675
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP TAS, OMIM ID: 181270
HumanBMPER168667BMP binding endothelial regulator
img HP RolledUp, OMIM ID: 608022
HumanTRPV3162514transient receptor potential cation channel, subfamily V, member 3
img HP TAS, OMIM ID: 614594
HumanMPLKIP136647M-phase specific PLK1 interacting protein
img HP RolledUp, OMIM ID: 234050
HumanEVC2132884Ellis van Creveld syndrome 2
img HP TAS, OMIM ID: 225500
HumanEDARADD128178EDAR-associated death domain
img HP TAS, OMIM ID: 224900
img HP TAS, OMIM ID: 129490
HumanGJB4127534gap junction protein, beta 4, 30.3kDa
img HP TAS, OMIM ID: 133200
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP TAS, OMIM ID: 257980
HumanCARD1479092caspase recruitment domain family, member 14
img HP TAS, OMIM ID: 173200
HumanWNK165125WNK lysine deficient protein kinase 1
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanDCLRE1C64421DNA cross-link repair 1C
img HP TAS, OMIM ID: 603554
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP TAS, OMIM ID: 277590
img HP TAS, OMIM ID: 117550
HumanFAM111A63901family with sequence similarity 111, member A
img HP TAS, OMIM ID: 602361
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
img HP TAS, OMIM ID: 201100
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001231Abnormality of the fingernails0self