Human Phenotype Ontology 
Grandparent Node:
expandDuplication of phalanx of hand (HP:0009997)help
Parent Node:
expandAbnormality of the proximal phalanx of the 4th finger (HP:0009284)help
Parent Node:
expandDuplication of phalanx of 4th finger (HP:0009972)help
Parent Node:
expandDuplication of the proximal phalanx of hand (HP:0010006)help
..Starting node
..expandDuplication of the proximal phalanx of the 4th finger (HP:0009977)help
Term ID: 9977
Name: Duplication of the proximal phalanx of the 4th finger
Synonym: Duplication of the proximal bone of the ring finger; Partial/complete duplication of the proximal phalanx of the 4th finger
Definition: Partial or complete duplication of the fourth proximal phalanx of hand.
Comments:
Reference: HP:0009977
Genes and Diseases:
 
       Child Nodes:
........expandComplete duplication of the proximal phalanx of the 4th finger (HP:0009980) help
........expandPartial duplication of the proximal phalanx of the 4th finger (HP:0009983) 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 2nd finger (HP:0009947) help
..expandDuplication of the proximal phalanx of the 3rd finger (HP:0009964) 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:0009977HP:0009977Duplication of the proximal phalanx of the 4th finger0 CL E G H
HP:0009977HP:0009983Partial duplication of the proximal phalanx of the 4th finger1 CL E G H
HP:0009977HP:0009980Complete duplication of the proximal phalanx of the 4th 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.