Human Phenotype Ontology 
Grandparent Node:
expandSynostosis involving bones of the feet (HP:0009140)help
Grandparent Node:
expandSynostosis involving digits (HP:0100262)help
Parent Node:
expandProximal symphalangism (HP:0100264)help
Parent Node:
expandSymphalangism affecting the phalanges of the toes (HP:0010179)help
Parent Node:
expandSynostosis involving bones of the toes (HP:0100235)help
..Starting node
..expandProximal foot symphalangism (HP:0100237)help
Term ID: 100237
Name: Proximal foot symphalangism
Synonym:
Definition:
Comments:
Reference: HP:0100237
Genes and Diseases:
 
       Child Nodes:
........expandProximal/middle symphalangism of 3rd toe (HP:0100480) help
........expandProximal/middle symphalangism of 4th toe (HP:0100481) help
........expandProximal/middle symphalangism of 5th toe (HP:0100482) help
........expandSynostosis of the proximal phalanx of the hallux with the 1st metatarsal (HP:0100488) help
........expandProximal/middle symphalangism of 2nd toe (HP:0100489) help

 Sister Nodes: 
..expandDistal foot symphalangism (HP:0001859) help
..expandSecond toe symphalangism (HP:0010353) help
..expandSymphalangism affecting the phalanges of the 3rd toe (HP:0010365) help
..expandSymphalangism affecting the phalanges of the 4th toe (HP:0010377) help
..expandSymphalangism affecting the phalanges of the 5th toe (HP:0010389) help
..expandSymphalangism affecting the phalanges of the hallux (HP:0010064) 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:0100237HP:0100237Proximal foot symphalangism0NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122
HP:0100237HP:0100489Proximal/middle symphalangism of 2nd toe1 CL E G H
HP:0100237HP:0100488Synostosis of the proximal phalanx of the hallux with the 1st metatarsal1 CL E G H
HP:0100237HP:0100480Proximal/middle symphalangism of 3rd toe1 CL E G H
HP:0100237HP:0100482Proximal/middle symphalangism of 5th toe1NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122
HP:0100237HP:0100481Proximal/middle symphalangism of 4th toe1NOG 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.