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Details
Link-It Detail - Human Phenotype - Abnormality of calcium homeostasis
Debug Stats
  • ### Total Build Time: 51 ms 29.924 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 211 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=5 ms Completed: 5 ms rowSize= 813 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.668 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 2.126 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=24 ms Completed: 24 ms rowSize= 23.753 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of calcium homeostasis HP:0004363
Definition (1)
An abnormality of `calcium ion homeostasis` (GO:0055074).
Parents (2)
img Abnormality of metabolism/homeostasis HP:0001939
img Abnormality of divalent inorganic cation homeostasis HP:0010927
Children (5)
img Hypercalciuria HP:0002150
img Hypocalcemia HP:0002901
img Hypercalcemia HP:0003072
img Hypocalciuria HP:0003127
img Elevated calcitonin HP:0003528
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of divalent inorganic cation homeostasis HP:0010927
Genes (95)

Species:
human : 95
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
img HP RolledUp, OMIM ID: 612089
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanGNAS-AS1149775
img HP RolledUp, OMIM ID: 603233
HumanCLDN19149461claudin 19
img HP RolledUp, OMIM ID: 248190
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img HP RolledUp, OMIM ID: 241530
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
img HP RolledUp, OMIM ID: 602014
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanCDC7379577cell division cycle 73
img HP RolledUp, OMIM ID: 608266
img HP RolledUp, OMIM ID: 145000
img HP RolledUp, OMIM ID: 145001
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
HumanFAM111A63901family with sequence similarity 111, member A
img HP RolledUp, OMIM ID: 127000
img HP RolledUp, OMIM ID: 602361
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
HumanADCY1055811adenylate cyclase 10 (soluble)
img HP RolledUp, OMIM ID: 143870
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanTMEM12755654transmembrane protein 127
img HP RolledUp, OMIM ID: 171300
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
HumanDGCR854487DGCR8 microprocessor complex subunit
img HP RolledUp, OMIM ID: 192430
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanKIF1B23095kinesin family member 1B
img HP RolledUp, OMIM ID: 171300
HumanCLDN1610686claudin 16
img HP RolledUp, OMIM ID: 248250
HumanDGCR29993DiGeorge syndrome critical region gene 2
img HP RolledUp, OMIM ID: 192430
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img HP RolledUp, OMIM ID: 214800
HumanPREPL9581prolyl endopeptidase-like
img HP RolledUp, OMIM ID: 606407
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004363Abnormality of calcium homeostasis0self