Human Phenotype Ontology 
Grandparent Node:
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Abnormal foot morphology (HP:0001760)help
Grandparent Node:
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Aplasia/hypoplasia involving bones of the lower limbs (HP:0006493)help
Parent Node:
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Aplasia/Hypoplasia involving bones of the feet (HP:0006494)help
..Starting node
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Partial absence of foot (HP:0030032)help
Term ID: 30032
Name: Partial absence of foot
Synonym: Partial absence of foot
Definition: An incomplete absence of the foot, with no bony elements distal to the tarsals, but with preservation of some or all of the tarsals.
Comments:
Reference: HP:0030032
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent foot (HP:0011301) help
..expandAplasia/Hypoplasia of metatarsal bones (HP:0001964) help
..expandAplasia/Hypoplasia of the phalanges of the toes (HP:0010173) help
..expandAplasia/Hypoplasia of the tarsal bones (HP:0008363) help
..expandAplasia/Hypoplasia of toe (HP:0001991) help
..expandLower limb peromelia (HP:0009820) help
..expandShort foot (HP:0001773) 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:0030032HP:0030032Partial absence of foot0GLI3 CL E G H27374319ORPHA:93322Tibial hemimeliaHP:0040283 - Occasional270


Genes (1) :GLI3

Diseases (1) :ORPHA:93322
 

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