raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:85196

Nodulosis-arthropathy-osteolysis syndrome

inactive · moved to ORPHA:371428Multicentric osteolysis-nodulosis-arthropathy spectrum

Synonyms: NAO syndrome

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 Multicentric osteolysis-nodulosis-arthropathy spectrum

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNodulosis-arthropathy-osteolysis syndromeNAO syndrome
frSyndrome de nodulose-arthropathie-ostéolyseSyndrome NAO
deNodulose-Arthropathie-Osteolyse-Syndrom
esSíndrome de nodulosis-artropatía-osteólisisSíndrome NAO
itSindrome nodulosi-artropatia-osteolisiOsteolisi multicentrica - nodulosi - artropatia · Sindrome NAO
nlNodulosis - artropathie - osteolyse-syndroomMulticentrische osteolyse - nodulosis - artropathie-syndroom · NAO-syndroom
ptSíndrome nodulose - artropatia - osteólise
plZespół guzki-artropatia-osteolizaOsteoliza policentryczna - guzki - artropatia · Zespół NAO
csSyndrom zahrnující nodulózu, artropatii a osteolýzuSyndrom zahrnující multicentrickou osteolýzu, nodulózu a artropatii · NAO syndrom
ukСиндром нодулозу-артропатії-остеолізуСиндром NAO
zh结节病-关节病-骨溶解综合征NAO综合征
trNodüloz-artropati-osteoliz sendromuNAO 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