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Details
Link-It Detail - Human Phenotype - Abnormality of the nail
Debug Stats
  • ### Total Build Time: 31 ms 39.880 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 198 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 192 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= 779 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 11.212 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.021 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 23.343 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the nail HP:0001597
Definition (1)
Abnormality of the `nail` (FMA:54326).
Parents (2)
img Abnormality of the integument HP:0001574
img Abnormality of skin adnexa HP:0011138
Children (35)
img Hyperconvex nail HP:0001795
img Fragile nails HP:0001808
img Broad nail HP:0001821
img Nail pits HP:0001803
img Pterygium formation (nails) HP:0002165
img Tubular nails, fifth fingers HP:0008380
img Split nail HP:0001809
img Nail dystrophy HP:0008404
img Abnormality of the periungual region HP:0100803
img Congenital curved nail of fourth toe HP:0008393
img Circumungual hyperkeratosis HP:0008399
img Neoplasm of the nail HP:0100826
img Paronychia HP:0001818
img Aplasia/Hypoplasia of the nails HP:0008386
img Leukonychia HP:0001820
img Nail bed telangiectasia HP:0001232
img Abnormality of the toenails HP:0008388
img Abnormality of nail color HP:0100643
img Ridged nail HP:0001807
img Abnormality of the fingernails HP:0001231
img Thick nail HP:0001805
img Onychogryposis HP:0001819
img Small nails HP:0001813
img Concave nail HP:0001598
img Slow-growing nails HP:0008383
img Recurrent loss of toenails and fingernails HP:0008390
img Abnormality of the subungual region HP:0009723
img Pyramidal skinfold extending from the base to the top of the nails HP:0009758
img Chronic monilial nail infection HP:0008396
img Thin nail HP:0001816
img Nail dysplasia HP:0002164
img Short nail HP:0001799
img Onycholysis HP:0001806
img Short, thin, slow growing nails HP:0008411
img Bifid nail HP:0010793
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the integument HP:0001574
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of skin adnexa HP:0011138
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of skin adnexa HP:0011138
Genes (265)

Species:
human : 265
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
HumanECTD6101101770Ectodermal dysplasia 6, hair/nail type
img HP RolledUp, OMIM ID: 614928
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
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanNDNC9100682325Nail disorder, nonsyndromic congenital, 9
img HP RolledUp, OMIM ID: 614149
HumanMDNS100529148Mammary-digital-nail syndrome
img HP RolledUp, OMIM ID: 613689
HumanDUP17Q23.1Q23.2100526743
img HP RolledUp, OMIM ID: 613618
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanAGSPX100188767Angio serpiginosum
img HP RolledUp, OMIM ID: 300652
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanSHFM3100049542Split-hand/foot malformation 3
img HP RolledUp, OMIM ID: 246560
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanPSORS10503613psoriasis susceptibility 10
img HP RolledUp, OMIM ID: 177900
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanPSORS9359825psoriasis susceptibility 9
img HP RolledUp, OMIM ID: 177900
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanRSPO4343637R-spondin 4
img HP RolledUp, OMIM ID: 206800
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP IEA, OMIM ID: 181270
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP IEA, OMIM ID: 243800
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001597Abnormality of the nail0self