Human Phenotype Ontology 
Grandparent Node:
expandAbnormal bone structure (HP:0003330)help
Parent Node:
expandFibrous dysplasia of the bones (HP:0010734)help
..Starting node
..expandPolyostotic fibrous dysplasia (HP:0010735)help
Term ID: 10735
Name: Polyostotic fibrous dysplasia
Synonym:
Definition: Fibrous dysplasia of the bones were lesions are localized in many bones throughout of the body. Polyostotic fibrous dysplasia is a cardinal feature of McCune-Albright syndrome.
Comments:
Reference: HP:0010735
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMonostotic fibrous dysplasia (HP:0010736) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010735HP:0010735Polyostotic fibrous dysplasia0GNAS CL E G H27784392ORPHA:562McCune-Albright syndromeHP:0040283 - Occasional101
HP:0010735HP:0010735Polyostotic fibrous dysplasia0GNAS CL E G H27784392OMIM:174800McCune-Albright syndrome, somatic, mosaic.101


Genes (1) :GNAS

Diseases (2) :ORPHA:562 OMIM:174800
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.