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Details
Link-It Detail - Human Phenotype - Abnormality of the alveolar ridges
Debug Stats
  • ### Total Build Time: 23 ms 21.983 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 286 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= 445 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.693 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 16.039 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the alveolar ridges HP:0006477
Definition (1)
Any abnormality of the alveolar ridges (on the upper or lower jaws). The alveolar ridges contain the sockets (alveoli) of the teeth.
Parents (1)
img Abnormality of the teeth HP:0000164
Children (8)
img Alveolar process hypoplasia HP:0006329
img Broad alveolar ridges HP:0000187
img Alveolar ridge overgrowth HP:0009085
img Fibrous syngnathia HP:0009754
img Atrophy of alveolar ridges HP:0006308
img Midline notch of upper alveolar ridge HP:0009084
img Progressive alveolar ridge hypertropy HP:0009092
img Alveolar ridge cleft HP:0010289
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300004
HumanEVC2132884Ellis van Creveld syndrome 2
img HP IEA, OMIM ID: 225500
HumanDIS3L2129563DIS3 mitotic control homolog (S. cerevisiae)-like 2
img HP RolledUp, OMIM ID: 267000
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
img HP RolledUp, OMIM ID: 252500
HumanCMDR64588Craniometaphyseal dysplasia, autosomal recessive
img HP RolledUp, OMIM ID: 218400
HumanZC4H255906zinc finger, C4H2 domain containing
img HP RolledUp, OMIM ID: 314580
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 605039
img HP RolledUp, OMIM ID: 211750
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
img HP RolledUp, OMIM ID: 216340
HumanOFD18481oral-facial-digital syndrome 1
img HP RolledUp, OMIM ID: 311200
HumanTBX156913T-box 15
img HP RolledUp, OMIM ID: 260660
HumanIRF63664interferon regulatory factor 6
img HP RolledUp, OMIM ID: 119500
HumanGPC32719glypican 3
img HP RolledUp, OMIM ID: 312870
HumanGJA12697gap junction protein, alpha 1, 43kDa
img HP RolledUp, OMIM ID: 164200
img HP RolledUp, OMIM ID: 218400
HumanGPC42239glypican 4
img HP RolledUp, OMIM ID: 312870
HumanEVC2121Ellis van Creveld syndrome
img HP IEA, OMIM ID: 225500
HumanDHCR24171824-dehydrocholesterol reductase
img HP RolledUp, OMIM ID: 602398
HumanDHCR717177-dehydrocholesterol reductase
img HP RolledUp, OMIM ID: 270400
HumanCTSC1075cathepsin C
img HP RolledUp, OMIM ID: 245000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006477Abnormality of the alveolar ridges0self