ConductScience.org, home
Papers
API referenceFor AI assistants

Paper · 42412262

When X Does Not Mark the Spot: Autosomal Dominant and Recessive Forms of Renal Hypophosphatemic Rickets and Osteomalacia.

Ferreira CR and 1 other. Curr Osteoporos Rep, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Download JSON
Cite this record

ConductScience Library. When X Does Not Mark the Spot: Autosomal Dominant and Recessive Forms of Renal Hypophosphatemic Rickets and Osteomalacia. Papers, record 42412262. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42412262

On this page

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
When X Does Not Mark the Spot: Autosomal Dominant and Recessive Forms of Renal Hypophosphatemic Rickets and Osteomalacia.
PubMed
Journal
Curr Osteoporos Rep
PubMed
Year
2026
PubMed
Publication types
Journal Article, Review
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2026-08-13
PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Ferreira CRCarlos Rhttps://orcid.org/0000-0002-2697-1046
2Imel EAErik Ahttps://orcid.org/0000-0002-7284-3467

Source PubMed

Topics9

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
OsteomalaciaMajor topic
Fibroblast Growth FactorsMajor topic
Familial Hypophosphatemic RicketsMajor topic
Rickets, HypophosphatemicMajor topic
Humans
Fibroblast Growth Factor-23
Genes, Recessive
Genes, Dominant
Rickets

Source PubMed

Grants1

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
ZIA HD009024Intramural NIH HHSUnited StatesZIAHD009024PubMed

Source NIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References97

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
126,857,895Treatment of hypophosphatemic rickets in generalized arterial calcification of infancy (GACI) without worsening of vascular calcification.Am J Med Genet A2016https://conductscience.org/library/papers/26857895PubMed
219,555,782Hypophosphatemia induced by intravenous administration of saccharated ferric oxide: another form of FGF23-related hypophosphatemia.Bone2009https://conductscience.org/library/papers/19555782PubMed
317,315,533Hypophosphatemic rickets in opsismodysplasia.J Pediatr Endocrinol Metab2007https://conductscience.org/library/papers/17315533PubMed
434,882,836Musculoskeletal Comorbidities and Quality of Life in ENPP1-Deficient Adults and the Response of Enthesopathy to Enzyme Replacement Therapy in Murine Models.J Bone Miner Res2022https://conductscience.org/library/papers/34882836PubMed
538,364,990An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).Kidney Int2024https://conductscience.org/library/papers/38364990PubMed
635,999,193Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome.Genes Chromosomes Cancer2022https://conductscience.org/library/papers/35999193PubMed
726,186,302Iron Supplementation Associated With Loss of Phenotype in Autosomal Dominant Hypophosphatemic Rickets.J Clin Endocrinol Metab2015https://conductscience.org/library/papers/26186302PubMed
824,006,476Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.Hum Mol Genet2014https://conductscience.org/library/papers/24006476PubMed
922,006,328Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice.Proc Natl Acad Sci U S A2011https://conductscience.org/library/papers/22006328PubMed
1029,654,216Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.J Am Soc Nephrol2018https://conductscience.org/library/papers/29654216PubMed

1 to 10 of 97

See all 97 references

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes26

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
AVPR2554PubTator's text mininghttps://conductscience.org/library/genes/554NCBI Gene
CASR846PubTator's text mininghttps://conductscience.org/library/genes/846NCBI Gene
CYP24A11,591PubTator's text mininghttps://conductscience.org/library/genes/1591NCBI Gene
DMP11,758PubTator's text mininghttps://conductscience.org/library/genes/1758NCBI Gene
ENPP15,167PubTator's text mininghttps://conductscience.org/library/genes/5167NCBI Gene
EPAS12,034PubTator's text mininghttps://conductscience.org/library/genes/2034NCBI Gene
EPO2,056PubTator's text mininghttps://conductscience.org/library/genes/2056NCBI Gene
FAM20C56,975PubTator's text mininghttps://conductscience.org/library/genes/56975NCBI Gene
FGF12,246PubTator's text mininghttps://conductscience.org/library/genes/2246NCBI Gene
FGF238,074PubTator's text mininghttps://conductscience.org/library/genes/8074NCBI Gene

1 to 10 of 26

See all 26 genes

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/42412262

GET https://conductscience.org/api/papers/v1/42412262/references?page=2

API referenceFor AI assistants