Human Phenotype Ontology 
Grandparent Node:
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Abnormality of bone mineral density (HP:0004348)help
Grandparent Node:
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Abnormality of the tarsal bones (HP:0001850)help
Parent Node:
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Abnormal tarsal bone mineral density (HP:0009132)help
..Starting node
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Osteoporotic tarsals (HP:0008076)help
Term ID: 8076
Name: Osteoporotic tarsals
Synonym:
Definition: Reduction in bone mineral density affecting any or all of the tarsal bones, seven bones of the foot comprising the calcaneus, talus, cuboid, navicular, and the cuneiform bones.
Comments:
Reference: HP:0008076
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandTarsal sclerosis (HP:0031051) 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:0008076HP:0008076Osteoporotic tarsals0 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.