(Q4118166)

English

polyostotic fibrous dysplasia

autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty

osteitis fibrosa disseminata
Fibrous Dysplasia, Polyostotic
McCune Albright syndrome

In more languages

edit

Statements

instance of

class of disease

0 references

subclass of

fibrous dysplasia of bone

0 references

autosomal genetic disease

1 reference

30 November 2020

1 reference

30 November 2020

0 references

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

ICD-9-CM

756.54

1 reference

15 May 2019

C34610

1 reference

15 May 2019

C48627

1 reference

15 May 2019

http://purl.obolibrary.org/obo/DOID_1858

1 reference

30 November 2020

http://identifiers.org/doid/DOID:1858

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

Commons category

McCune-Albright syndrome

0 references

Identifiers

MeSH descriptor ID

D005359

subject named as

Fibrous Dysplasia, Polyostotic

1 reference

15 May 2019

C05.116.099.708.375.381

0 references

PatientsLikeMe condition ID

0 references

0 references

1 reference

30 November 2020

1 reference

imported from Wikimedia project

1 reference

15 May 2019

1 reference

15 May 2019

Microsoft Academic ID

0 references

1 reference

15 May 2019

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

0 references

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

0 references

Polyostotic fibrous dysplasia

0 references

Sitelinks

Wikipedia(4 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:McCune-Albright syndrome