Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the tarsal bones (HP:0001850)help
Parent Node:
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Abnormal talus morphology (HP:0008365)help
..Starting node
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Tarsal osteovalgus (HP:0001775)help
Term ID: 1775
Name: Tarsal osteovalgus
Synonym:
Definition:
Comments:
Reference: HP:0001775
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDelayed talus ossification (HP:0011836) help
..expandOsteolysis of talus (HP:0008095) help
..expandRocker bottom foot (HP:0001838) help
..expandShortening of the talar neck (HP:0008117) 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:0001775HP:0001775Tarsal osteovalgus0EPB41L1 CL E G H20363378OMIM:614257MENTAL RETARDATION, AUTOSOMAL DOMINANT 11; MRD1129


Genes (1) :EPB41L1

Diseases (1) :OMIM:614257
 

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