raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93275

Thanatophoric dysplasia, Glasgow variant

inactive · moved to ORPHA:175Cartilage-hair hypoplasia

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cartilage-hair hypoplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enThanatophoric dysplasia, Glasgow variant
frNanisme thanatophore type Glasgow
deKleinwuchs, thanatophorer, Glasgow-Variante
esDisplasia tanatofórica, variante de Glasgow
itDisplasia tanatofora, variante Glasgow
nlThanatofore dysplasie, Glasgow-variant
ptDisplasia tanatofórica, tipo Glasgow
plDysplazja tanatoforyczna wariant Glasgow
csThanatoforická dysplázie, Glasgowská varianta
ukТанатофорна дисплазія, варіант Глазго
zh致死性侏儒症,Glasgow变异型
trTanatoforik displazi, Glasgow varyantı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM273680Evalidated
MeSHC536506Evalidated
UMLSC1848865Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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