Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the 3rd toe (HP:0010330)help
Grandparent Node:
expandTriangular shaped phalanges of the toes (HP:0010180)help
Parent Node:
expandProximal foot symphalangism (HP:0100237)help
Parent Node:
expandSymphalangism affecting the middle phalanx of the 5th toe (HP:0100472)help
Parent Node:
expandSymphalangism affecting the proximal phalanx of the 5th toe (HP:0100475)help
Parent Node:
expandTriangular shaped phalanges of the 3rd toe (HP:0010366)help
..Starting node
..expandProximal/middle symphalangism of 5th toe (HP:0100482)help
Term ID: 100482
Name: Proximal/middle symphalangism of 5th toe
Synonym: Fused innermost and middle little toe bones; Fused innermost and middle pinkie toe bones; Fused innermost and middle pinky toe bones; Symphalangism of the middle and proximal phalanges of the 5th toe
Definition: Bony fusion of the middle and proximal phalanges of the 5th toe.
Comments:
Reference: HP:0100482
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProximal/middle symphalangism of 2nd toe (HP:0100489) help
..expandSymphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal (HP:0100485) 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:0100482HP:0100482Proximal/middle symphalangism of 5th toe0NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122


Genes (1) :NOG

Diseases (1) :OMIM:186500
 

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