intestinal hypomagnesemia 1
type: Thing
description: human disease
additional property: PropertyValue
  property ID: P31
  value: rare disease
additional property: PropertyValue
  property ID: P31
  value: class of disease
additional property: PropertyValue
  property ID: P279
  value: Neonatal hypocalcemia
additional property: PropertyValue
  property ID: P279
  value: primary hypomagnesemia
additional property: PropertyValue
  property ID: P492
  value: 602014
additional property: PropertyValue
  property ID: P699
  value: DOID:0060883
additional property: PropertyValue
  property ID: P1550
  value: 30924
additional property: PropertyValue
  property ID: P1995
  value: endocrinology
additional property: PropertyValue
  property ID: P2293
  value: TRPM6
additional property: PropertyValue
  property ID: P2888
  value: http://purl.obolibrary.org/obo/DOID_0060883
additional property: PropertyValue
  property ID: P2888
  value: http://identifiers.org/doid/DOID:0060883
additional property: PropertyValue
  property ID: P2888
  value: http://www.orpha.net/ORDO/Orphanet_30924
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additional property: PropertyValue
  property ID: P4229
  value: E83.4
additional property: PropertyValue
  property ID: P4317
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additional property: PropertyValue
  property ID: P5008
  value: WikiProject Medicine
additional property: PropertyValue
  property ID: P5270
  value: MONDO_0011176
additional property: PropertyValue
  property ID: P6366
  value: 2780028369
additional property: PropertyValue
  property ID: P7464
  value: hypomagnesemia-with-secondary-hypocalcemia
additional property: PropertyValue
  property ID: P11430
  value: DI-00576
confidence:
  popularity graph score:
    score: 0.001
    score pct: 0
    tier: established
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 6
      unique citations norm: 0.002
      monthly pageviews: 215
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 6
  monthly pageviews: 215
  yearly pageviews: 235
  pageview trend:
    m: 2026-07
    v: 215
  pageview trend:
    m: 2026-06
    v: 16
  pageview trend:
    m: 2026-05
    v: 4
  tier: established
claims:
  P31:
    value: Q929833
    source count: 0
    confidence: 0.0
    value label: rare disease
  P31:
    value: Q112193867
    source count: 0
    confidence: 0.0
    value label: class of disease
  P279:
    value: Q18391768
    source count: 0
    confidence: 0.0
    value label: Neonatal hypocalcemia
  P279:
    value: Q32136684
    source count: 1
    confidence: 0.2
    value label: primary hypomagnesemia
  P492:
    value: 602014
    source count: 1
    confidence: 0.2
  P699:
    value: DOID:0060883
    source count: 1
    confidence: 0.2
  P1550:
    value: 30924
    source count: 1
    confidence: 0.2
  P1995:
    value: Q162606
    source count: 1
    confidence: 0.2
    value label: endocrinology
  P2293:
    value: Q14914571
    source count: 3
    confidence: 0.6
    value label: TRPM6
  P2888:
    value: http://purl.obolibrary.org/obo/DOID_0060883
    source count: 1
    confidence: 0.2
  P2888:
    value: http://identifiers.org/doid/DOID:0060883
    source count: 1
    confidence: 0.2
  P2888:
    value: http://www.orpha.net/ORDO/Orphanet_30924
    source count: 0
    confidence: 0.0
  P2892:
    value: C1865974
    source count: 1
    confidence: 0.2
  P4229:
    value: E83.4
    source count: 1
    confidence: 0.2
  P4317:
    value: 13072
    source count: 0
    confidence: 0.0
  P5008:
    value: Q4099686
    source count: 0
    confidence: 0.0
    value label: WikiProject Medicine
  P5270:
    value: MONDO_0011176
    source count: 0
    confidence: 0.0
  P6366:
    value: 2780028369
    source count: 0
    confidence: 0.0
  P7464:
    value: hypomagnesemia-with-secondary-hypocalcemia
    source count: 0
    confidence: 0.0
  P11430:
    value: DI-00576
    source count: 0
    confidence: 0.0
citations:
  source: Open Targets Platform
  stated in qid: Q113138000
  retrieved: 2023-08-24
citations:
  source: Identifiers.org
  stated in qid: Q16335166
citations:
  source: Disease Ontology
  stated in qid: Q5282129
  retrieved: 2020-11-30
citations:
  source: UMLS 2023
  stated in qid: Q118645236
  retrieved: 2023-06-16
citations:
  source: Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia
  stated in qid: Q28200829
citations:
  source: Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
  stated in qid: Q28200813
meta:
  wikidata id: Q17028486
  domain: rare_disease
  level: standard
  html url: https://4ort.xyz/entity/intestinal-hypomagnesemia-1
  markdown url: https://4ort.xyz/entity/intestinal-hypomagnesemia-1.md
  facts url summary: https://4ort.xyz/entity/intestinal-hypomagnesemia-1/facts.json
  facts url standard: https://4ort.xyz/entity/intestinal-hypomagnesemia-1/facts.json
  facts url full: https://4ort.xyz/entity/intestinal-hypomagnesemia-1/facts.json
  data source: Wikidata (CC0 / public domain)
  license: https://creativecommons.org/publicdomain/zero/1.0/
  api version: v1
  served at: 2026-08-05T12:05:28.827196Z
  entity updated at: 2026-05-03T21:19:00.258443+00:00Z
  entity created at: 2026-05-03T14:24:04.502882+00:00Z