raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79429

OBSOLETE: Familial spinal 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 spinal neurofibromatosis
frOBSOLETE : Neurofibromatose spinale
deOBSOLET: Neurofibromatose, familiäre spinale
esOBSOLETO: Neurofibromatosis espinal familiar
itOBSOLETO: Neurofibromatosi familiare spinale
nlOBSOLEET: Familiale spinale neurofibromatose
ptOBSOLETO: Neurofibromatose espinhal familiar
plNIEAKTUALNE: Rodzinna nerwiakowlókniakowatosc rdzenia
csNEAKTUÁLNÍ: Familiární spinální neurofibromatóza
ukЗАСТАРІЛО: Сімейний нейрофіброматоз хребта
zh弃用:家族性脊髓神经纤维瘤病
trEski adı: Ailesel spinal 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