raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79428

OBSOLETE: Familial segmental neurofibromatosis

inactive · referred to ORPHA:636Neurofibromatosis type 1

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Neurofibromatosis type 1

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Familial segmental neurofibromatosis
frOBSOLETE : Neurofibromatose segmentaire
deOBSOLET: Neurofibromatose, familiäre segmentale
esOBSOLETO: Neurofibromatosis segmentaria familiar
itOBSOLETO: Neurofibromatosi familiare segmentale
nlOBSOLEET: Familiale segmentale neurofibromatose
ptOBSOLETO: Neurofibromatose segmentar familiar
plNIEAKTUALNE: Rodzinna nerwiakowlókniakowatosc segmentalna
csNEAKTUÁLNÍ: Familiární segmentální neurofibromatóza
ukЗАСТАРІЛО: Сімейний сегментарний нейрофіброматоз
zh弃用:家族性节段性神经纤维瘤病
trEski adı: Ailesel segmental nörofibromatoz
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