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Details
Link-It Detail - Human Phenotype - Abnormality of phalangeal joints of the hand
Debug Stats
  • ### Total Build Time: 38 ms 35.818 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 219 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
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  • 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= 781 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 4.762 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 5.826 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 23.071 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of phalangeal joints of the hand HP:0006261
Parents (2)
img Abnormality of phalanx of finger HP:0005918
img Abnormal joint morphology HP:0001367
Children (14)
img Prominent interphalangeal joints HP:0006237
img Soft tissue swelling of interphalangeal joints HP:0006162
img Camptodactyly of finger HP:0100490
img Osteoarthritis of the small joints of the hand HP:0004268
img Narrow small joints of the hand HP:0004267
img Enlarged metacarpophalangeal joints HP:0006163
img Interphalangeal joint erosions HP:0006252
img Limited mobility of proximal interphalangeal joint HP:0006217
img Limited interphalangeal movement HP:0006064
img Swelling of proximal interphalangeal joints HP:0006253
img Enlarged interphalangeal joints HP:0006247
img Reduced proximal interphalangeal joint space HP:0006019
img Subluxation of the small joints of the hand HP:0004269
img Camptodactyly (hands) HP:0010563
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011811img Abnormality of phalanx of finger HP:0005918
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of phalanx of finger HP:0005918
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of phalanx of finger HP:0005918
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of phalanx of finger HP:0005918
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal joint morphology HP:0001367
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormal joint morphology HP:0001367
Genes (156)

Species:
human : 156
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanCAMPD1100381210Camptodactyly 1
img HP RolledUp, OMIM ID: 114200
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanDUPC1780895Dupuytren contracture 1
img HP RolledUp, OMIM ID: 126900
HumanACRPV414058Acropectorovertebral dysplasia (F syndrome)
img HP RolledUp, OMIM ID: 102510
HumanDOK7285489docking protein 7
img HP RolledUp, OMIM ID: 208150
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanCANT1124583calcium activated nucleotidase 1
img HP RolledUp, OMIM ID: 251450
HumanANTXR2118429anthrax toxin receptor 2
img HP RolledUp, OMIM ID: 236490
HumanMRSS114890Mental retardation, X-linked, with short stature
img HP RolledUp, OMIM ID: 300360
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 191900
HumanATPAF291647ATP synthase mitochondrial F1 complex assembly factor 2
img HP RolledUp, OMIM ID: 604273
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
img HP RolledUp, OMIM ID: 612350
HumanSCARF291179scavenger receptor class F, member 2
img HP RolledUp, OMIM ID: 600920
HumanMEGF1084466multiple EGF-like-domains 10
img HP RolledUp, OMIM ID: 614399
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006261Abnormality of phalangeal joints of the hand0self