Human Phenotype Ontology 
Grandparent Node:
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Abnormal middle phalanx morphology of the hand (HP:0009833)help
Grandparent Node:
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Abnormal proximal phalanx morphology of the hand (HP:0009834)help
Grandparent Node:
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Duplication of phalanx of hand (HP:0009997)help
Parent Node:
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Abnormality of the middle phalanx of the 2nd finger (HP:0009543)help
Parent Node:
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Duplication of phalanx of 2nd finger (HP:0009945)help
Parent Node:
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Duplication of the middle phalanx of hand (HP:0010008)help
..Starting node
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Duplication of the middle phalanx of the 2nd finger (HP:0009949)help
Term ID: 9949
Name: Duplication of the middle phalanx of the 2nd finger
Synonym: Partial/complete duplication of the middle bone of the index finger; Partial/complete duplication of the middle phalanx of the 2nd finger
Definition: Partial or complete duplication of the middle phalanx of index finger.
Comments:
Reference: HP:0009949
Genes and Diseases:
 
       Child Nodes:
........expandComplete duplication of the middle phalanx of the 2nd finger (HP:0009952) help
........expandPartial duplication of the middle phalanx of the 2nd finger (HP:0009953) help

 Sister Nodes: 
..expandComplete duplication of the middle phalanges of the hand (HP:0010002) help
..expandDuplication of the middle phalanx of the 3rd finger (HP:0009963) help
..expandDuplication of the middle phalanx of the 4th finger (HP:0009976) help
..expandDuplication of the middle phalanx of the 5th finger (HP:0009989) help
..expandDuplication of the proximal phalanx of the thumb (HP:0009613) help
..expandPartial duplication of the middle phalanges of the hand (HP:0010005) 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:0009949HP:0009949Duplication of the middle phalanx of the 2nd finger0 CL E G H
HP:0009949HP:0009953Partial duplication of the middle phalanx of the 2nd finger1 CL E G H
HP:0009949HP:0009952Complete duplication of the middle 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.