Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the distal phalanx of the 5th finger (HP:0004225)help
Grandparent Node:
expandDuplication of phalanx of 5th finger (HP:0009985)help
Grandparent Node:
expandDuplication of the distal phalanx of hand (HP:0009883)help
Parent Node:
expandComplete duplication of the distal phalanges of the hand (HP:0010001)help
Parent Node:
expandComplete duplication of the phalanges of the 5th finger (HP:0009986)help
Parent Node:
expandDuplication of the distal phalanx of the 5th finger (HP:0009988)help
..Starting node
..expandComplete duplication of the distal phalanx of the 5th finger (HP:0009991)help
Term ID: 9991
Name: Complete duplication of the distal phalanx of the 5th finger
Synonym: Complete duplication of the outermost little finger bone; Complete duplication of the outermost pinkie finger bone; Complete duplication of the outermost pinky finger bone
Definition: Complete duplication of the distal phalanx of little finger.
Comments:
Reference: HP:0009991
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPartial duplication of the distal phalanx of the 5th finger (HP:0009994) 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:0009991HP:0009991Complete duplication of the distal phalanx of the 5th finger0 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.