raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2676

Neuroectodermal-endocrine syndrome

inactive · moved to ORPHA:3464Woodhouse-Sakati syndrome

Synonyms: Oerter-Friedman-Anderson syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Woodhouse-Sakati syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNeuroectodermal-endocrine syndromeOerter-Friedman-Anderson syndrome
frSyndrome neuroectodermique endocrineSyndrome d'Oerter-Friedman-Anderson
deNeuroektodermales endokrines SyndromOerter-Friedman-Anderson-Syndrom
esSíndrome neuroectodérmico-endocrino
itSindrome neuroectodermica endocrinaSindrome di Oerter-Friedman-Anderson
nlNeuro-ectodermaal-endocrien syndroomOerter-Friedman-Andersonsyndroom
ptSíndrome neuroectodérmico endócrinoSíndrome Oerter-Friedman-Anderson
plZespół neuroektodermalno-endokrynologicznyZespół Oertera, Friedmana i Andersona
csNeuroektodermální-endokrinní syndromOerterové-Friedmanův-Andersonův syndrom · Oerter-Friedman-Andersonův syndrom
ukНейроектодермально-ендокринний синдромСиндром Ортера-Фрідмана-Андерсона
zh神经外胚层-内分泌综合征Oerter-Friedman-Anderson综合征
trNöroektodermal-endokrin sendromOerter-Friedman-Anderson 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