Human Phenotype Ontology 
Grandparent Node:
expandPhenotypic abnormality (HP:0000118)help
Parent Node:
expandAbnormality of the skeletal system (HP:0000924)help
..Starting node
..expandobsolete Abnormality of the periosteum (HP:0040166)help
Term ID: 40166
Name: obsolete Abnormality of the periosteum
Synonym:
Definition:
Comments:
Reference: HP:0040166
Genes and Diseases:
 
       Child Nodes:
........expandAbnormal periosteum morphology (HP:0030313) help
................... HP:0006051 Metacarpal periosteal thickening
................... HP:0006175 Proximal phalangeal periosteal thickening
................... HP:0006465 Periosteal thickening of long tubular bones
................... HP:0008074 Metatarsal periosteal thickening
................... HP:0030314 Periostosis
................... HP:0031485 Subperiosteal bone formation
................... HP:0040165 Periostitis

 Sister Nodes: 
..expandAbnormal musculoskeletal physiology (HP:0011843) help
..expandAbnormal nasal skeleton morphology (HP:0010937) help
..expandAbnormal odontoid tissue morphology (HP:3000050) help
..expandAbnormal skeletal morphology (HP:0011842) help
..expandAbnormality of limb bone (HP:0040068) help
..expandEctopic calcification (HP:0010766) 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:0040166HP:0040166obsolete Abnormality of the periosteum0 CL E G H


Genes (0) :

Diseases (0) :
 

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