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Details
Link-It Detail - Human Phenotype - Abnormality of the gingiva
Debug Stats
  • ### Total Build Time: 31 ms 29.109 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 220 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
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 1 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 451 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.931 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 22.996 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the gingiva HP:0000168
Definition (1)
Any abnormality of the `gingiva` (FMA:59762) (also known as gums).
Parents (1)
img Abnormality of the oral cavity HP:0000163
Children (9)
img Gingival fibromatosis HP:0000169
img Gingivitis HP:0000230
img Gingival hyperkeratosis HP:0000222
img Periodontitis HP:0000165
img Fusion of gums HP:0012292
img Gingival overgrowth HP:0000212
img Gingival hypertrophy HP:0000195
img Periodontitis HP:0000704
img Gingival bleeding HP:0000225
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the oral cavity HP:0000163
Genes (98)

Species:
human : 98
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
img HP RolledUp, OMIM ID: 135400
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
img HP RolledUp, OMIM ID: 130080
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP RolledUp, OMIM ID: 203300
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
img HP RolledUp, OMIM ID: 234500
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
HumanEDARADD128178EDAR-associated death domain
img HP RolledUp, OMIM ID: 129490
HumanANTXR2118429anthrax toxin receptor 2
img HP RolledUp, OMIM ID: 228600
img HP RolledUp, OMIM ID: 236490
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanHPS489781Hermansky-Pudlak syndrome 4
img HP RolledUp, OMIM ID: 203300
HumanHPS384343Hermansky-Pudlak syndrome 3
img HP RolledUp, OMIM ID: 203300
HumanDTNBP184062dystrobrevin binding protein 1
img HP RolledUp, OMIM ID: 203300
HumanHPS679803Hermansky-Pudlak syndrome 6
img HP RolledUp, OMIM ID: 203300
HumanGINGF264644gingival fibromatosis, hereditary, 2
img HP RolledUp, OMIM ID: 135300
HumanFAM20C56975family with sequence similarity 20, member C
img HP RolledUp, OMIM ID: 259775
HumanFERMT155612fermitin family member 1
img HP RolledUp, OMIM ID: 173650
HumanSLC35C155343solute carrier family 35 (GDP-fucose transporter), member C1
img HP RolledUp, OMIM ID: 266265
HumanSAMD954809sterile alpha motif domain containing 9
img HP RolledUp, OMIM ID: 610455
HumanFAM20A54757family with sequence similarity 20, member A
img HP RolledUp, OMIM ID: 614253
HumanTMCO154499transmembrane and coiled-coil domains 1
img HP RolledUp, OMIM ID: 614132
HumanRIN254453Ras and Rab interactor 2
img HP RolledUp, OMIM ID: 613075
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanCD20930835CD209 molecule
img HP RolledUp, OMIM ID: 614371
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000168Abnormality of the gingiva0self