Homepage > Rare diseases > Search

Search for a rare disease

*
(*) mandatory field

Polyostotic fibrous dysplasia

Suggest an update
Your message has been sent Your message has not been sent. Please contact an administrator.

ORPHA:93276

Classification level: Subtype of disorder

Prevalence: -

Inheritance: Unknown

Age of onset:

ICD-10: Q78.1

ICD-11: FB80.0

UMLS: C0016065

MeSH: D005359

GARD: 4213

MedDRA: 10036120

Summary

This disease is described under Fibrous dysplasia of bone

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Guidelines
Emergency guidelines
Français (2015.pdf) - Orphanet Urgences
Español (2017.pdf) - Orphanet Urgences
Disease review articles
Review article
English (2012) - Orphanet J Rare Dis
Clinical genetics review
English (2024) - GeneReviews
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.