Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the toes (HP:0010161)help
Parent Node:
expandAbnormality of the phalanges of the 4th toe (HP:0010336)help
Parent Node:
expandTriangular shaped phalanges of the toes (HP:0010180)help
..Starting node
..expandTriangular shaped phalanges of the 4th toe (HP:0010378)help
Term ID: 10378
Name: Triangular shaped phalanges of the 4th toe
Synonym: Triangular shaped bones of 4th toe
Definition:
Comments:
Reference: HP:0010378
Genes and Diseases:
 
       Child Nodes:
........expandProximal/middle symphalangism of 3rd toe (HP:0100480) help
........expandSymphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal (HP:0100483) help
........expandSymphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal (HP:0100486) help

 Sister Nodes: 
..expandTriangular shaped distal phalanges of the toes (HP:0010192) help
..expandTriangular shaped middle phalanges of the toes (HP:0010201) help
..expandTriangular shaped phalanges of the 2nd toe (HP:0010354) help
..expandTriangular shaped phalanges of the 3rd toe (HP:0010366) help
..expandTriangular shaped phalanges of the 5th toe (HP:0010390) help
..expandTriangular shaped phalanges of the hallux (HP:0010065) help
..expandTriangular shaped proximal phalanges of the toes (HP:0010210) 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:0010378HP:0010378Triangular shaped phalanges of the 4th toe0MAP3K20 CL E G H5177617797ORPHA:488232Split-foot malformation-mesoaxial polydactyly syndrome2
HP:0010378HP:0100486Symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal1 CL E G H
HP:0010378HP:0100480Proximal/middle symphalangism of 3rd toe1 CL E G H
HP:0010378HP:0100483Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal1MAP3K20 CL E G H5177617797ORPHA:488232Split-foot malformation-mesoaxial polydactyly syndrome2


Genes (1) :MAP3K20

Diseases (1) :ORPHA:488232
 

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