raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3333

Connective tissue dysplasia, Spellacy type

inactive · moved to ORPHA:2909Rothmund-Thomson syndrome

Synonyms: Spellacy-Gibbs-Watts syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Rothmund-Thomson syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enConnective tissue dysplasia, Spellacy typeSpellacy-Gibbs-Watts syndrome
frDysplasie du tissu conjonctif type SpellacySyndrome de Spellacy-Gibbs-Watts
deBindegewebsdysplasie Typ SpellacySkelettdysplasie - Teleangiektasie - mesodermale Dysgenesie der Iris · Spellacy-Gibbs-Watts-Syndrom
esDisplasia del tejido conjuntivo tipo Spellacy
itDisplasia del tessuto connettivo, tipo SpellacySindrome di Spellacy-Gibbs-Watts
nlBindweefseldysplasie, Spellacy-typeSpellacy-Gibbs-Wattssyndroom
ptDisplasia do tecido conjuntivo, tipo SpellacySíndrome Spellacy-Gibbs-Watts
plDysplzja tkanki łącznej typu SpellacyZespół Spellacy, Gibbsa i Wattsa
csPojivová dysplázie, Spellacyové typSpellacyové-Gibbsové-Wattsův syndrom · Spellacy-Gibbs-Wattsův syndrom
ukДисплазія сполучної тканини, тип СпелласіСиндром Спелласі-Гіббса-Уоттса
zh结缔组织发育不良Spellacy亚型Spellacy-Gibbs-Watts综合征
trBağ dokusu displazisi, Spellacy tipiYazım-Gibbs-Watts 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.

7

Sources for this card