Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the 5th toe (HP:0010342)help
Grandparent Node:
expandAplasia/Hypoplasia of the phalanges of the toes (HP:0010173)help
Parent Node:
expandAbnormal morphology of the proximal phalanx of the 5th toe (HP:0010394)help
Parent Node:
expandAplasia/hypoplasia of proximal toe phalanx (HP:0010203)help
Parent Node:
expandAplasia/Hypoplasia of the 5th toe (HP:0010343)help
Parent Node:
expandAplasia/Hypoplasia of the phalanges of the 5th toe (HP:0010383)help
..Starting node
..expandAplasia/hypoplasia of the proximal phalanx of the 5th toe (HP:0100377)help
Term ID: 100377
Name: Aplasia/hypoplasia of the proximal phalanx of the 5th toe
Synonym: Absent/small innermost little toe bone; Absent/small innermost pinkie toe bone; Absent/small innermost pinky toe bone; Absent/underdeveloped innermost 5th toe bone
Definition: Absence (agenesis) or underdevelopment of the proximal phalanx of the 5th toe.
Comments:
Reference: HP:0100377
Genes and Diseases:
 
       Child Nodes:
........expandAplasia of the proximal phalanx of the 5th toe (HP:0100386) help
........expandShort proximal phalanx of the 5th toe (HP:0100397) help

 Sister Nodes: 
..expandAplasia of the phalanges of the 5th toe (HP:0100364) help
..expandAplasia/Hypoplasia of the distal phalanx of the 5th toe (HP:0100371) help
..expandAplasia/Hypoplasia of the middle phalanx of the 5th toe (HP:0100374) help
..expandShort phalanx of the 5th toe (HP:0100368) 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:0100377HP:0100377Aplasia/hypoplasia of the proximal phalanx of the 5th toe0 CL E G H
HP:0100377HP:0100397Short proximal phalanx of the 5th toe1 CL E G H
HP:0100377HP:0100386Aplasia of the proximal phalanx of the 5th toe1 CL E G H


Genes (0) :

Diseases (0) :
 

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