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Details
Link-It Detail - Human Phenotype - Abnormality of the parathyroid physiology
Debug Stats
  • ### Total Build Time: 29 ms 25.992 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 216 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 457 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.065 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.172 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 21.705 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.035 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the parathyroid physiology HP:0011767
Definition (1)
A functional abnormality of the `parathyroid gland` (FMA:13890).
Parents (1)
img Abnormality of the parathyroid gland HP:0000828
Children (3)
img Pseudohypoparathyroidism HP:0000852
img Hypoparathyroidism HP:0000829
img Hyperparathyroidism HP:0000843
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the parathyroid gland HP:0000828
Genes (48)

Species:
human : 48
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanGNAS-AS1149775
img HP RolledUp, OMIM ID: 603233
HumanCDC7379577cell division cycle 73
img HP RolledUp, OMIM ID: 145001
img HP RolledUp, OMIM ID: 608266
HumanFAM111A63901family with sequence similarity 111, member A
img HP RolledUp, OMIM ID: 127000
HumanIRX510265iroquois homeobox 5
img HP RolledUp, OMIM ID: 611174
HumanGCM29247glial cells missing homolog 2 (Drosophila)
img HP RolledUp, OMIM ID: 146200
HumanHHC39151hypocalciuric hypercalcemia 3 (Oklahoma type)
HumanSTX168675syntaxin 16
img HP RolledUp, OMIM ID: 603233
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanTBCE6905tubulin folding cofactor E
img HP RolledUp, OMIM ID: 241410
HumanRET5979ret proto-oncogene
img HP RolledUp, OMIM ID: 171400
HumanPTH1R5745parathyroid hormone 1 receptor
img HP RolledUp, OMIM ID: 156400
HumanPTH5741parathyroid hormone
img HP RolledUp, OMIM ID: 146200
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
img HP RolledUp, OMIM ID: 274600
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img HP RolledUp, OMIM ID: 309000
HumanTRNW4578tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNV4577tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNS24575tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNS14574tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNQ4572tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNL14567tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNK4566tRNA
img HP RolledUp, OMIM ID: 540000
HumanTRNF4558tRNA
img HP RolledUp, OMIM ID: 540000
HumanRNR14549s-rRNA
img HP RolledUp, OMIM ID: 540000
HumanND64541NADH dehydrogenase, subunit 6 (complex I)
img HP RolledUp, OMIM ID: 540000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011767Abnormality of the parathyroid physiology0self