Human Phenotype Ontology 
Grandparent Node:
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Abnormal 5th finger morphology (HP:0004207)help
Grandparent Node:
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Hand polydactyly (HP:0001161)help
Grandparent Node:
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Postaxial polydactyly (HP:0100259)help
Parent Node:
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Postaxial hand polydactyly (HP:0001162)help
..Starting node
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Postaxial polydactyly type A (HP:0005696)help
Term ID: 5696
Name: Postaxial polydactyly type A
Synonym:
Definition: Supernumerary digits located at the ulnar side of the hand with a complete extra finger and extra metacarpal.
Comments:
Reference: HP:0005696
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral postaxial polydactyly (HP:0006136) help
..expandRudimentary postaxial polydactyly of hands (HP:0005676) 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:0005696HP:0005696Postaxial polydactyly type A0KIAA0825 CL E G H28560028532OMIM:618498Polydactyly, postaxial, type A10
HP:0005696HP:0005696Postaxial polydactyly type A0WDPCP CL E G H5105728027OMIM:217085Congenital heart defects, hamartomas of tongue, and polysyndactyly60


Genes (2) :KIAA0825 WDPCP

Diseases (2) :OMIM:618498 OMIM:217085
 

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