Human Phenotype Ontology 
Grandparent Node:
expandDuplication of the proximal phalanx of hand (HP:0010006)help
Grandparent Node:
expandPartial duplication of the phalanx of hand (HP:0009999)help
Parent Node:
expandDuplication of the proximal phalanx of the 5th finger (HP:0009990)help
Parent Node:
expandPartial duplication of the phalanges of the 5th finger (HP:0009987)help
Parent Node:
expandPartial duplication of the proximal phalanges of the hand (HP:0010003)help
..Starting node
..expandPartial duplication of the proximal phalanx of the 5th finger (HP:0009996)help
Term ID: 9996
Name: Partial duplication of the proximal phalanx of the 5th finger
Synonym: Partial duplication of the innermost little finger bone; Partial duplication of the innermost pinkie finger bone; Partial duplication of the innermost pinky finger bone
Definition: Partial or complete duplication of the fifth proximal phalanx of hand, seen on x-rays as a broad and/or bifid phalanx.
Comments:
Reference: HP:0009996
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBifid first metacarpal (HP:0009616) help
..expandPartial duplication of the proximal phalanx of the 2nd finger (HP:0009955) help
..expandPartial duplication of the proximal phalanx of the 3rd finger (HP:0009970) help
..expandPartial duplication of the proximal phalanx of the 4th finger (HP:0009983) 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:0009996HP:0009996Partial 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.