raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1417

OBSOLETE: Platyspondylic lethal chondrodysplasia

inactive · referred to ORPHA:93434Spondylodysplastic dysplasia

Synonyms: OBSOLETE: Akaba-Hayasaka 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 Spondylodysplastic dysplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Platyspondylic lethal chondrodysplasiaOBSOLETE: Akaba-Hayasaka syndrome
frOBSOLETE : Chondrodysplasie platyspondylique létaleOBSOLETE : Syndrome d'Akaba-Hayasaka
deOBSOLET: Letale Chondrodysplasie mit PlatyspondylieOBSOLET: Akaba-Hayasaka-Syndrom
esOBSOLETO: Condrodisplasia platispondílica letalOBSOLETO: Síndrome de Akaba-Hayasaka
itOBSOLETO: Condrodisplasia letale con platispondiliaOBSOLETO: Sindrome di Akaba-Hayasaka
nlOBSOLEET: Platyspondylische letale chondrodysplasieOBSOLEET: Syndroom van Akaba-Hayasaka
ptOBSOLETO: Condrodisplasia platiespondilítica letalOBSOLETO: Síndrome Akaba-Hayasaka
plNIEAKTUALNE: Smiertelna chondrodysplazja platyspondylicznaNIEAKTUALNE: Zespół Akaba i Hayasaka
csNEAKTUÁLNÍ: Platyspondylická letální chondrodysplázie= en
ukЗАСТАРІЛО: Платиспондилярна летальна хондродисплазіяЗАСТАРІЛО: Синдром Акаба-Хаясака
zh弃用：椎骨体扁平致死性软骨发育异常Akaba-Hayasaka综合征
trEski adı: Platyspondilik letal kondrodisplaziAkaba-Hayasaka 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