raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:623

NAME syndrome

inactive · moved to ORPHA:1359Carney complex

Synonyms: Nevi-atrial myxoma-myxoid neurofibromata-ephelides 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 Carney complex

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNAME syndromeNevi-atrial myxoma-myxoid neurofibromata-ephelides syndrome
frSyndrome NAMESyndrome de naevi-myxome de l'oreillette-neurofibrome myxoïde-éphélides
deNAME-SyndromNaevi - atriales Myxom - myxoides Neurofibrom - Epheliden
esSíndrome NAME
itSindrome NAMENevi - mixoma atriale - neurofibromi mixoidi - efelidi
nlNAME-syndroomNaevi - atriummyxoom - myxoïde neurofibromata - efeliden-syndroom
ptSíndrome NAMESíndrome de nevo-mixoma auricular-neurofibromas mixóides-efélides
plZespół NAMEZnamię - śluzak przedsionka - nerwiakowłókniak śluzowaty - piegi
csNAME syndromSyndrom zahrnující névy, atriální myxom, myxoidní neurofibromy a ephelides
ukNAME синдромСиндром міксоми неві-передсердь-міксоїдної нейрофіброми-ефеліди
zhNAME综合征痣-心房粘液瘤-粘液样神经纤维瘤-雀斑综合征
trNAME sendromuNevi-atriyal miksoma-miksoid neurofibromata-ephelides 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