Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the distal phalanx of the thumb (HP:0009617)help
Grandparent Node:
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Duplication of the distal phalanx of hand (HP:0009883)help
Grandparent Node:
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Duplication of thumb phalanx (HP:0009942)help
Parent Node:
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Complete duplication of the distal phalanges of the hand (HP:0010001)help
Parent Node:
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Complete duplication of thumb phalanx (HP:0009943)help
Parent Node:
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Duplication of the distal phalanx of the thumb (HP:0009612)help
..Starting node
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Complete duplication of distal phalanx of the thumb (HP:0009606)help
Term ID: 9606
Name: Complete duplication of distal phalanx of the thumb
Synonym: Complete duplication of outermost bone of the thumb
Definition: Complete duplication of the distal phalanx of the thumb. On x-ray two separate bones appear side to side.
Comments:
Reference: HP:0009606
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBifid distal phalanx of the thumb (HP:0009611) 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:0009606HP:0009606Complete duplication of distal phalanx of the thumb0BMPR1B CL E G H6581077ORPHA:93384Brachydactyly type CHP:0040282 - Frequent90
HP:0009606HP:0009606Complete duplication of distal phalanx of the thumb0GDF5 CL E G H82004220ORPHA:93384Brachydactyly type CHP:0040282 - Frequent52
HP:0009606HP:0009606Complete duplication of distal phalanx of the thumb0LMBR1 CL E G H6432713243OMIM:174500Polydactyly, preaxial II.106


Genes (3) :BMPR1B GDF5 LMBR1

Diseases (2) :ORPHA:93384 OMIM:174500
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.