Rothmund–Thomson syndrome
Rothmund–Thomson syndrome (RTS), is a rare autosomal recessive skin condition. There have been several reported cases associated with osteosarcoma. A hereditary basis, mutations in the DNA helicase RECQL4 gene, causing problems during initiation of DNA replication has been implicated in the syndrome.
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ErythrokeratodermaPoikiloderma congenitalePoikiloderma of Rothmund-ThomsonPoikiloderma of Rothmund–ThomsonRothmund-Thompson's syndromeRothmund-Thompson syndromeRothmund-Thomson SyndromeRothmund-Thomson syndromeRothmund-thomson syndromeRothmund thomson syndromeSymmetrical progressive of Gottron erythrokeratodermaThomson SyndomeThomson Syndrome
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August von RothmundBaller–Gerold syndromeBloom syndromeCancer syndromeCellular senescenceChromosome 8DNA damage theory of agingDNA repair-deficiency disorderErythrokeratodermaEvolution of ageingHelicaseHomologous recombinationKindler syndromeList of MeSH codes (C16)List of MeSH codes (C17)List of MeSH codes (C18)List of OMIM disorder codesList of diseases (P)List of diseases (R)List of genes mutated in cutaneous conditionsList of radiographic findings associated with cutaneous conditionsList of skin conditionsList of syndromesMatthew Sydney ThomsonOsteosarcomaPoikilodermaPoikiloderma congenitalePoikiloderma of Rothmund-ThomsonPoikiloderma of Rothmund–ThomsonPoikiloderma vasculare atrophicansProgeroid syndromesRAPADILINO syndromeRECQL4RecQ helicaseRothmundRothmund-Thompson's syndromeRothmund-Thompson syndromeRothmund-Thomson SyndromeRothmund-Thomson syndromeRothmund-thomson syndrome
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Rothmund–Thomson syndrome
Rothmund–Thomson syndrome (RTS), is a rare autosomal recessive skin condition. There have been several reported cases associated with osteosarcoma. A hereditary basis, mutations in the DNA helicase RECQL4 gene, causing problems during initiation of DNA replication has been implicated in the syndrome.
has abstract
Das Rothmund-Thomson-Syndrom ( ...... Hautkrankheit (Genodermatose).
@de
La sindrome di Rothmund-Thomso ...... io di sviluppare osteosarcomi.
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Le syndrome de Rothmund-Thomso ...... mission autosomique récessive.
@fr
Rothmund–Thomson syndrome (RTS ...... en implicated in the syndrome.
@en
Zespół Rothmunda-Thompsona (an ...... pecyficznego leczenia zespołu.
@pl
متلازمة روثموند - تومسون (بالإ ...... العظمية في العديد من الحالات.
@ar
DiseasesDB
eMedicine subject
derm
@en
eMedicine topic
379
@en
geneReviewsId
geneReviewsName
Rothmund-Thomson Syndrome
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ICD10
ICD9
MeSH ID
OMIM id
Link from a Wikipage to an external page
Wikipage page ID
12,994,627
page length (characters) of wiki page
Wikipage revision ID
993,127,448
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caption
Panel showing some clinical fe ...... tinuity of the cortical bone .
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DiseasesDB
eMedicineSubj
derm
@en
eMedicineTopic
GeneReviewsName
Rothmund-Thomson Syndrome
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GeneReviewsNBK
NBK1237
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ICD
MeshID
D011038
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name
Rothmund–Thomson syndrome
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OMIM
Orphanet
synonyms
Poikiloderma atrophicans with cataract or Poikiloderma congenitale
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wikiPageUsesTemplate
wordnet_type
subject
hypernym
comment
Das Rothmund-Thomson-Syndrom ( ...... Hautkrankheit (Genodermatose).
@de
La sindrome di Rothmund-Thomso ...... io di sviluppare osteosarcomi.
@it
Le syndrome de Rothmund-Thomso ...... mission autosomique récessive.
@fr
Rothmund–Thomson syndrome (RTS ...... en implicated in the syndrome.
@en
Zespół Rothmunda-Thompsona (an ...... horowania na kostniakomięsaka.
@pl
متلازمة روثموند - تومسون (بالإ ...... العظمية في العديد من الحالات.
@ar
label
Rothmund-Thomson-Syndrom
@de
Rothmund–Thomson syndrome
@en
Sindrome di Rothmund-Thomson
@it
Syndrome de Rothmund-Thomson
@fr
Zespół Rothmunda-Thomsona
@pl
متلازمة روثموند تومسون
@ar
로트문드-톰슨 증후군
@ko
sameAs
wasDerivedFrom
isPrimaryTopicOf
name
Rothmund–Thomson syndrome
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