raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2161

OBSOLETE: Holoacardius amorphus

inactive · referred to ORPHA:93890Rare developmental defect during embryogenesis

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 Rare developmental defect during embryogenesis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Holoacardius amorphus
frOBSOLETE : Holoacardius amorphus
deOBSOLET: Holocardius amorphus
esOBSOLETO: Holoacardius amorphus
itOBSOLETO: Olocardio amorfo
nlOBSOLEET: Holoacardius amorphus
ptOBSOLETO: Holoacardius amorphus
plNIEAKTUALNE: Amorficzny plód bez serca
csNEAKTUÁLNÍ: Holoacardius amorphus
ukЗАСТАРІЛО: Holoacardius amorphus
zh弃用:无定形无心寄生胎畸胎
trEski adı: Holoakardiyus amorfus
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