Human Phenotype Ontology 
Grandparent Node:
expandAplasia/Hypoplasia of the 5th toe (HP:0010343)help
Grandparent Node:
expandAplasia/Hypoplasia of the phalanges of the 5th toe (HP:0010383)help
Grandparent Node:
expandHypoplasia of the phalanges of the toes (HP:0010746)help
Parent Node:
expandAplasia/Hypoplasia of the middle phalanx of the 5th toe (HP:0100374)help
Parent Node:
expandShort phalanx of the 5th toe (HP:0100368)help
..Starting node
..expandShort middle phalanx of the 5th toe (HP:0100394)help
Term ID: 100394
Name: Short middle phalanx of the 5th toe
Synonym: Hypoplastic/small middle phalanx of the 5th toe; Short middle bone of little toe; Short middle bone of pinkie toe; Short middle bone of pinky toe; Short middle phalanx of the fifth toe
Definition: Developmental hypoplasia of the middle phalanx of the 5th toe.
Comments:
Reference: HP:0100394
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandShort distal phalanx of the 5th toe (HP:0100391) help
..expandShort proximal phalanx of the 5th toe (HP:0100397) 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:0100394HP:0100394Short middle phalanx of the 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.