Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the proximal phalanx of the 5th finger (HP:0009150)help
Grandparent Node:
expandDuplication of phalanx of 5th finger (HP:0009985)help
Grandparent Node:
expandDuplication of the proximal phalanx of hand (HP:0010006)help
Parent Node:
expandComplete duplication of the phalanges of the 5th finger (HP:0009986)help
Parent Node:
expandComplete duplication of the proximal phalanges of the hand (HP:0010000)help
Parent Node:
expandDuplication of the proximal phalanx of the 5th finger (HP:0009990)help
..Starting node
..expandComplete duplication of the proximal phalanx of the 5th finger (HP:0009993)help
Term ID: 9993
Name: Complete duplication of the proximal phalanx of the 5th finger
Synonym: Complete duplication of the innermost little finger bone; Complete duplication of the innermost pinkie finger bone; Complete duplication of the innermost pinky finger bone
Definition: Complete duplication of the fifth proximal phalanx of hand.
Comments:
Reference: HP:0009993
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPartial duplication of the proximal phalanx of the 5th finger (HP:0009996) 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:0009993HP:0009993Complete duplication of the proximal 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.