Human Phenotype Ontology 
Grandparent Node:
expandDuplication of phalanx of hand (HP:0009997)help
Parent Node:
expandAbnormality of the proximal phalanx of the 2nd finger (HP:0009544)help
Parent Node:
expandDuplication of phalanx of 2nd finger (HP:0009945)help
Parent Node:
expandDuplication of the proximal phalanx of hand (HP:0010006)help
..Starting node
..expandDuplication of the proximal phalanx of the 2nd finger (HP:0009947)help
Term ID: 9947
Name: Duplication of the proximal phalanx of the 2nd finger
Synonym: Duplication of the proximal bone of the index finger; Partial/complete duplication of the proximal phalanx of the 2nd finger
Definition: Partial or complete duplication of the second proximal phalanx of hand.
Comments:
Reference: HP:0009947
Genes and Diseases:
 
       Child Nodes:
........expandComplete duplication of the proximal phalanx of the 2nd finger (HP:0009954) help
........expandPartial duplication of the proximal phalanx of the 2nd finger (HP:0009955) help

 Sister Nodes: 
..expandComplete duplication of the proximal phalanges of the hand (HP:0010000) help
..expandDuplication of the 1st metacarpal (HP:0009609) help
..expandDuplication of the proximal phalanx of the 3rd finger (HP:0009964) help
..expandDuplication of the proximal phalanx of the 4th finger (HP:0009977) help
..expandDuplication of the proximal phalanx of the 5th finger (HP:0009990) help
..expandPartial duplication of the proximal phalanges of the hand (HP:0010003) 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:0009947HP:0009947Duplication of the proximal phalanx of the 2nd finger0 CL E G H
HP:0009947HP:0009955Partial duplication of the proximal phalanx of the 2nd finger1 CL E G H
HP:0009947HP:0009954Complete duplication of the proximal phalanx of the 2nd finger1 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.