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Details
Link-It Detail - Human Phenotype - Abnormality of the parathyroid morphology
Debug Stats
  • ### Total Build Time: 19 ms 11.124 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 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=4 ms Completed: 4 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=1 ms Completed: 1 ms rowSize= 457 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.082 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.172 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 6.820 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.035 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the parathyroid morphology HP:0011766
Definition (1)
A structural abnormality of the `parathyroid gland` (FMA:13890).
Parents (1)
img Abnormality of the parathyroid gland HP:0000828
Children (3)
img Neoplasm of the parathyroid gland HP:0100733
img Parathyroid dysgenesis HP:0011768
img Parathyroid hyperplasia HP:0008208
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the parathyroid gland HP:0000828
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
img HP RolledUp, OMIM ID: 612089
HumanFLCN201163folliculin
img HP RolledUp, OMIM ID: 135150
HumanCDC7379577cell division cycle 73
img HP RolledUp, OMIM ID: 608266
HumanCHD755636chromodomain helicase DNA binding protein 7
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
HumanTBX16899T-box 1
HumanRET5979ret proto-oncogene
img HP RolledUp, OMIM ID: 162300
HumanNF14763neurofibromin 1
HumanMSH24436mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
HumanMEN14221multiple endocrine neoplasia I
HumanDGCR1714DiGeorge syndrome chromosome region
HumanCCND1595cyclin D1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011766Abnormality of the parathyroid morphology0self