raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3133

OBSOLETE: Say-Field-Coldwell syndrome

inactive · referred to ORPHA:294959Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy

Synonyms: OBSOLETE: Triphalangeal thumbs-dislocation of patella syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Say-Field-Coldwell syndromeOBSOLETE: Triphalangeal thumbs-dislocation of patella syndrome
frOBSOLETE : Syndrome de Say-Field-ColdwellOBSOLETE : Syndrome de pouce triphalangé-luxation de la rotule
deOBSOLET: Say-Field-Coldwell-SyndromOBSOLET: Triphalangeale Daumen-Patella-Dislokation-Syndrom
esOBSOLETO: Síndrome de Say-Field-ColdwellOBSOLETO: Síndrome de pulgar trifalángico-luxación de rótula
itOBSOLETO: Sindrome di Say-Field-ColdwellOBSOLETO: Sindrome pollici trifalangei-dislocazione della rotula
nlOBSOLEET: Syndroom van Say-Field-ColdwellOBSOLEET: Trifalangeale duimen - luxatie van patella-syndroom
ptOBSOLETO: Síndrome Say-Field-ColdwellOBSOLETO: Síndrome de polegar trifalângico-luxação da rótula
plNIEAKTUALNE: Zespół Say'a, Fielda i ColdwellaNIEAKTUALNE: Trójpaliczkowe kciuki - przemieszczenie rzepki
csNEAKTUÁLNÍ: Sayův-Fieldův-Coldwellův syndromNEAKTUÁLNÍ: Syndrom zahrnující tříčlánkové palce ruky a dislokaci čéšky · NEAKTUÁLNÍ: Say-Field-Coldwellův syndrom
ukЗАСТАРІЛО: Синдром Сай-Філда-КолдуеллаСиндром трифалангового вивиху великих пальців - вивих надколінка
zhSay-Field-Coldwell综合征三指节拇指-髌骨脱位综合征
trSay-Field-Coldwell sendromuTrifalanjiyal başparmaklar-patella çıkığı sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

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Sources for this card