raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2615

Nakajo-Nishimura syndrome

inactive · moved to ORPHA:324977Proteasome-associated autoinflammatory syndrome

Synonyms: Amyotrophy-fat tissue anomaly syndrome · Secondary hypertrophic osteoperiostosis with pernio

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 Proteasome-associated autoinflammatory syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNakajo-Nishimura syndromeAmyotrophy-fat tissue anomaly syndrome · Secondary hypertrophic osteoperiostosis with pernio
frSyndrome de Nakajo-NishimuraOstéopériostite hypertrophique secondaire avec pernio · Syndrome d'amyotrophie-anomalie du tissu adipeux
deNakajo-Nishimura-SyndromSekundäre hypertrophe Osteoperiostose mit Pernio · Amyotrophie-Fettgewebeanomalie-Syndrom · NNS
esSíndrome de Nakajo-NishimuraOsteoperiostitis hipertrófica secundaria con pernio · Síndrome de amiotrofia-anomalía del tejido graso
itSindrome di Nakajo-NishimuraNNS · Osteoperiostite ipertrofica secondaria con eritema pernio · Sindrome amiotrofia-anomalia del tessuto adiposo
nlSyndroom van Nakajo-NishimuraAmyotrofie - vetweefselanomalie-syndroom · Secundaire hypertrofische osteoperiostose met pernio
ptSíndrome Nakajo-NishimuraAmiotrofia-anomalia do tecido adiposo
plZespół Nakajo i NishimuraNNS · Wtórny przerost kosto-okostnowy z odmrozinami · Zespół amiotrofia - nieprawidłowa tkanka tłuszczowa
csNakajoův-Nishimurův syndromNNS · Sekundární hypertrofní osteoperiostóza s oznobeninou · Syndrom zahrnující amyotrofii a anomálie tukové tkáně · Nakajo-Nishimurův syndrom
ukСиндром Накаджо-НішимураСиндром аміотрофії - аномалії жирової тканини · Вторинний гіпертрофічний остеоперіостоз з перніо
zhNakajo-Nishimura综合征继发性过度增殖骨周骨病伴冻疮
trNakajo-Nishimura sendromuAmyotrofi-yağ dokusu anomalisi sendromu · Perniyo ile seyreden sekonder hipertrofik osteoperiostoz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
GARD3916Evalidated

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