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 distal phalanx of the 5th toe (HP:0100371)help
Parent Node:
expandShort phalanx of the 5th toe (HP:0100368)help
..Starting node
..expandShort distal phalanx of the 5th toe (HP:0100391)help
Term ID: 100391
Name: Short distal phalanx of the 5th toe
Synonym: Hypoplastic/small distal phalanx of the 5th toe; Short distal phalanx of the fifth toe; Short outermost bone of the little toe; Short outermost bone of the pinkie toe; Short outermost bone of the pinky toe
Definition: Developmental hypoplasia of the distal phalanx of little toe.
Comments:
Reference: HP:0100391
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandShort middle phalanx of the 5th toe (HP:0100394) 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:0100391HP:0100391Short distal phalanx of the 5th toe0ARID1B CL E G H5749218040OMIM:135900Coffin-Siris syndrome 1.219


Genes (1) :ARID1B

Diseases (1) :OMIM:135900
 

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