Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the calf (HP:0002981)help
Grandparent Node:
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obsolete Abnormal morphology of bones of the lower limbs (HP:0040066)help
Parent Node:
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Abnormality of fibula morphology (HP:0002991)help
..Starting node
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Fibular duplication (HP:0010503)help
Term ID: 10503
Name: Fibular duplication
Synonym: Duplicated calf bone
Definition: Duplication of the fibula. This may occur as a part of diplopodia (accessory tarsal or metatarsal bone). Diplopodia with double fibula is an extremely rare condition.
Comments:
Reference: HP:0010503
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the fibula (HP:0006492) help
..expandDecreased fibular diameter (HP:0031107) help
..expandFibular bowing (HP:0010502) help
..expandFibular overgrowth (HP:0003099) help
..expandIncreased fibular diameter (HP:0012107) help
..expandLong fibula (HP:0003085) help
..expandSerpentine fibula (HP:0030045) help
..expandSynostosis involving the fibula (HP:0005928) help
..expandTibiofibular diastasis (HP:0100535) 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:0010503HP:0010503Fibular duplication0LMBR1 CL E G H6432713243ORPHA:2378Laurin-Sandrow syndromeHP:0040282 - Frequent106
HP:0010503HP:0010503Fibular duplication0LMBR1 CL E G H6432713243OMIM:135750Laurin-Sandrow syndrome.106
HP:0010503HP:0010503Fibular duplication0LMBR1 CL E G H6432713243OMIM:188740Tibia, hypoplasia or aplasia of, with polydactyly106


Genes (1) :LMBR1

Diseases (3) :ORPHA:2378 OMIM:135750 OMIM:188740
 

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