ORPHA:595216

Fibrous dysplasia/McCune-Albright syndrome

Synonyms: FD/MAS spectrum · FD/MAS syndrome · Fibrous dysplasia/McCune-Albright spectrum

Type: Clinical group
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Fibrous dysplasia/McCune-Albright syndrome	FD/MAS spectrum · FD/MAS syndrome · Fibrous dysplasia/McCune-Albright spectrum
fr	Syndrome de dysplasie fibreuse/McCune-Albright	MASFD · Spectre FD/MAS · Spectre dysplasie fibreuse/McCune-Albright · Syndrome FD/MAS
de	Fibröse Dysplasie/McCune-Albright-Syndrom	FD/MAS-Spektrum · FD/MAS-Syndrom · Fibröse Dysplasie/McCune-Albright-Spektrum
es	Síndrome de displasia fibrosa/McCune-Albright	Espectro DF/MAS · Espectro displasia fibrosa/McCune-Albright · Síndrome DF/MAS
it	Displasia fibrosa/sindrome di McCune-Albright	Sindrome FD/MAS · Spettro FD/MAS · Spettro della displasia fibrosa/sindrome di McCune-Albright
nl	Fibreuze dysplasie/Syndroom van McCune-Albright	FD/MAS-spectrum · FD/MAS-syndroom · Fibreuze dysplasie/Spectrum van McCune-Albright
pt	Displasia fibrosa/síndrome McCune-Albright	Espectro clínico FD/MAS · Espectro clínico de displasia fibrosa/McCune-Albright · Síndrome FD/MAS · Síndrome de displasia fibrosa/McCune-Albright
pl	Dysplazja włóknista/Zespół McCune’a i Albrighta	Dysplazja włóknista/Spektrum McCune’a i Albrighta
cs	Fibrózní dysplázie/McCuneův-Albrightův syndrom	= en
uk	Фіброзна дисплазія/синдром МакКьюна-Олбрайта	Спектр FD/MAS · Синдром FD/MAS · Фіброзна дисплазія/Спектр МакКьюна-Олбрайта
zh	Fibrous dysplasia/McCune-Albright syndrome	= en
tr	Fibrous dysplasia/McCune-Albright syndrome	= en

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5680283	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93419Rare bone disease

Parents in the classifications (1):

ORPHA:93450Primary bone dysplasia with disorganized development of skeletal components
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/595216
This record as JSON: /data/d/595216.json