Human Phenotype Ontology 
Grandparent Node:
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Abnormal foot morphology (HP:0001760)help
Grandparent Node:
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Abnormal lower limb bone morphology (HP:0040069)help
Parent Node:
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Abnormality of the tarsal bones (HP:0001850)help
..Starting node
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Abnormality of the os naviculare pedis (HP:0100339)help
Term ID: 100339
Name: Abnormality of the os naviculare pedis
Synonym:
Definition:
Comments:
Reference: HP:0100339
Genes and Diseases:
 
       Child Nodes:
........expandMorbus Koehler (HP:0010888) help

 Sister Nodes: 
..expandAbnormal talus morphology (HP:0008365) help
..expandAbnormal tarsal bone mineral density (HP:0009132) help
..expandAbnormal tarsal ossification (HP:0008369) help
..expandAbnormality of the calcaneus (HP:0008364) help
..expandAplasia/Hypoplasia of the tarsal bones (HP:0008363) help
..expandDeformed tarsal bones (HP:0008119) help
..expandFlattening of the talar dome (HP:0008144) help
..expandIrregular tarsal bones (HP:0004688) help
..expandLarge tarsal bones (HP:0004679) help
..expandOsteolysis involving tarsal bones (HP:0006234) help
..expandTarsal synostosis (HP:0008368) 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:0100339HP:0100339Abnormality of the os naviculare pedis0 CL E G H
HP:0100339HP:0041149Fractured navicular bone of pes1 CL E G H
HP:0100339HP:0010888Morbus Koehler1 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.