Human Phenotype Ontology 
Grandparent Node:
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Abnormality of bone mineral density (HP:0004348)help
Parent Node:
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Patchy changes of bone mineral density (HP:0010658)help
Parent Node:
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Reduced bone mineral density (HP:0004349)help
..Starting node
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Patchy variation in bone mineral density (HP:0010659)help
Term ID: 10659
Name: Patchy variation in bone mineral density
Synonym: Patchy increased and decreased bone mineral density
Definition: Patchy (irregular) changes in bone mineral density with patches of bone showing an increased density side to side with patches that are affected by reduction of mineral density. This is sometimes referred to as a moth-eaten appearance on x-rays.
Comments:
Reference: HP:0010659
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGeneralized bone demineralization (HP:0006462) help
..expandOsteomalacia (HP:0002749) help
..expandOsteopenia (HP:0000938) help
..expandOsteoporosis (HP:0000939) help
..expandPatchy reduction of bone mineral density (HP:0010657) help
..expandRickets (HP:0002748) 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:0010659HP:0010659Patchy variation in bone mineral density0LBR CL E G H39306518OMIM:215140Greenberg dysplasia.70


Genes (1) :LBR

Diseases (1) :OMIM:215140
 

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