TARP syndrome
type: Thing
additional property: PropertyValue
  property ID: P31
  value: head and neck disease
additional property: PropertyValue
  property ID: P31
  value: developmental defect during embryogenesis
additional property: PropertyValue
  property ID: P31
  value: rare disease
additional property: PropertyValue
  property ID: P279
  value: genetic syndromic Pierre robin syndrome
additional property: PropertyValue
  property ID: P279
  value: rare syndrome with cardiac malformations
additional property: PropertyValue
  property ID: P279
  value: syndrome
additional property: PropertyValue
  property ID: P486
  value: C536942
additional property: PropertyValue
  property ID: P492
  value: 311900
additional property: PropertyValue
  property ID: P665
  value: H00943
additional property: PropertyValue
  property ID: P699
  value: DOID:0111780
additional property: PropertyValue
  property ID: P780
  value: micrognathism
additional property: PropertyValue
  property ID: P780
  value: isolated cleft palate
additional property: PropertyValue
  property ID: P780
  value: clubfoot
additional property: PropertyValue
  property ID: P1550
  value: 2886
additional property: PropertyValue
  property ID: P2293
  value: RBM10
additional property: PropertyValue
  property ID: P2671
  value: /g/11qplpvlt2
additional property: PropertyValue
  property ID: P2841
  value: congenital onset
additional property: PropertyValue
  property ID: P2888
  value: http://www.orpha.net/ORDO/Orphanet_2886
additional property: PropertyValue
  property ID: P2888
  value: http://purl.obolibrary.org/obo/DOID_0111780
additional property: PropertyValue
  property ID: P2888
  value: http://identifiers.org/doid/DOID:0111780
additional property: PropertyValue
  property ID: P2892
  value: C1839463
additional property: PropertyValue
  property ID: P4317
  value: 10089
additional property: PropertyValue
  property ID: P5270
  value: MONDO_0010711
additional property: PropertyValue
  property ID: P7807
  value: 194645275
additional property: PropertyValue
  property ID: P11430
  value: DI-02837
confidence:
  popularity graph score:
    score: 0.001
    score pct: 0
    tier: established
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 9
      unique citations norm: 0.004
      monthly pageviews: 0
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 9
  monthly pageviews: 0
  yearly pageviews: 2
  pageview trend:
    m: 2026-05
    v: 2
  tier: established
claims:
  P31:
    value: Q55789477
    source count: 1
    confidence: 0.2
    value label: head and neck disease
  P31:
    value: Q55788864
    source count: 1
    confidence: 0.2
    value label: developmental defect during embryogenesis
  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: Q55787783
    source count: 1
    confidence: 0.2
    value label: genetic syndromic Pierre robin syndrome
  P279:
    value: Q55785518
    source count: 1
    confidence: 0.2
    value label: rare syndrome with cardiac malformations
  P279:
    value: Q179630
    source count: 1
    confidence: 0.2
    value label: syndrome
  P279:
    value: Q18553438
    source count: 1
    confidence: 0.2
    value label: X-linked disease
  P486:
    value: C536942
    source count: 1
    confidence: 0.2
  P492:
    value: 311900
    source count: 1
    confidence: 0.2
  P665:
    value: H00943
    source count: 0
    confidence: 0.0
  P699:
    value: DOID:0111780
    source count: 1
    confidence: 0.2
  P780:
    value: Q1100988
    source count: 3
    confidence: 0.6
    value label: micrognathism
  P780:
    value: Q27677677
    source count: 3
    confidence: 0.6
    value label: isolated cleft palate
  P780:
    value: Q1162164
    source count: 2
    confidence: 0.4
    value label: clubfoot
  P780:
    value: Q757749
    source count: 2
    confidence: 0.4
    value label: atrial heart septal defect
  P780:
    value: Q4009452
    source count: 2
    confidence: 0.4
    value label: persistent left superior vena cava
  P1550:
    value: 2886
    source count: 1
    confidence: 0.2
  P2293:
    value: Q18032782
    source count: 3
    confidence: 0.6
    value label: RBM10
  P2671:
    value: /g/11qplpvlt2
    source count: 0
    confidence: 0.0
  P2841:
    value: Q21953121
    source count: 1
    confidence: 0.2
    value label: congenital onset
  P2888:
    value: http://www.orpha.net/ORDO/Orphanet_2886
    source count: 0
    confidence: 0.0
  P2888:
    value: http://purl.obolibrary.org/obo/DOID_0111780
    source count: 1
    confidence: 0.2

value: http://identifiers.org/doid/DOID:0111780
source count: 1
confidence: 0.2

value: C1839463
source count: 1
confidence: 0.2

value: Q87.8
source count: 1
confidence: 0.2

value: 10089
source count: 1
confidence: 0.2

value: MONDO_0010711
source count: 0
confidence: 0.0

value: 194645275
source count: 0
confidence: 0.0

value: DI-02837
source count: 0
confidence: 0.0

source: Open Targets Platform
stated in qid: Q113138000
retrieved: 2023-08-24

source: Identifiers.org
stated in qid: Q16335166

source: Monarch Disease Ontology release 2018-06-29
stated in qid: Q55345445
retrieved: 2018-07-28

source: Disease Ontology
stated in qid: Q5282129
retrieved: 2020-11-30

source: UniProt
stated in qid: Q905695
retrieved: 2019-08-13

source: Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate
stated in qid: Q30478683

source: First reported adult patient with TARP syndrome: A case report
stated in qid: Q93271086

source: RBM10: Structure, functions, and associated diseases
stated in qid: Q108806632

source: TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations
stated in qid: Q64043309

wikidata id: Q55782603
domain: head_and_neck_disease
level: standard
html url: https://4ort.xyz/entity/tarp-syndrome
markdown url: https://4ort.xyz/entity/tarp-syndrome.md
facts url summary: https://4ort.xyz/entity/tarp-syndrome/facts.json
facts url standard: https://4ort.xyz/entity/tarp-syndrome/facts.json
facts url full: https://4ort.xyz/entity/tarp-syndrome/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-31T23:41:05.547290Z
entity updated at: 2026-05-03T21:19:00.258443+00:00Z
entity created at: 2026-05-03T15:00:37.686400+00:00Z