Human Phenotype Ontology 
Grandparent Node:
expandAbnormal foot morphology (HP:0001760)help
Grandparent Node:
expandAbnormal lower limb bone morphology (HP:0040069)help
Parent Node:
expandAbnormal metatarsal morphology (HP:0001832)help
..Starting node
..expandSecond metatarsal posteriorly placed (HP:0008125)help
Term ID: 8125
Name: Second metatarsal posteriorly placed
Synonym:
Definition:
Comments:
Reference: HP:0008125
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal metatarsal ossification (HP:0008371) help
..expandAbnormality of metatarsal epiphysis (HP:0010630) help
..expandAbnormality of the fifth metatarsal bone (HP:0008089) help
..expandAbnormality of the first metatarsal bone (HP:0010054) help
..expandAbnormality of the fourth metatarsal bone (HP:0040035) help
..expandAbnormality of the second metatarsal bone (HP:0040034) help
..expandAbnormality of the third metatarsal bone (HP:0010672) help
..expandAplasia/Hypoplasia of metatarsal bones (HP:0001964) help
..expandBroad metatarsal (HP:0001783) help
..expandDistal tapering of metatarsals (HP:0008133) help
..expandDuplication of metatarsal bones (HP:0001449) help
..expandExpanded metatarsals with widened medullary cavities (HP:0008102) help
..expandFlattened metatarsal heads (HP:0005194) help
..expandMetatarsal diaphyseal endosteal sclerosis (HP:0008114) help
..expandMetatarsal osteolysis (HP:0001473) help
..expandMetatarsal periosteal thickening (HP:0008074) help
..expandMetatarsal synostosis (HP:0001440) help
..expandMetatarsus adductus (HP:0001840) help
..expandMetatarsus valgus (HP:0010508) help
..expandOsteoporotic metatarsal (HP:0004699) help
..expandThin metatarsal cortices (HP:0008078) help
..expandY-shaped metatarsals (HP:0010567) 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:0008125HP:0008125Second metatarsal posteriorly placed0ERCC6 CL E G H20743438OMIM:214150Cerebrooculofacioskeletal syndrome 1.199


Genes (1) :ERCC6

Diseases (1) :OMIM:214150
 

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