Human Phenotype Ontology 
Grandparent Node:
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Deviation of finger (HP:0004097)help
Grandparent Node:
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Ulnar deviation of the hand or of fingers of the hand (HP:0001193)help
Parent Node:
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Deviation of the 3rd finger (HP:0009317)help
Parent Node:
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Ulnar deviation of finger (HP:0009465)help
..Starting node
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Ulnar deviation of the 3rd finger (HP:0009463)help
Term ID: 9463
Name: Ulnar deviation of the 3rd finger
Synonym: Ulnar deviation of middle fingers
Definition: Displacement of the 3rd finger towards the ulnar side (i.e., towards the ring finger).
Comments:
Reference: HP:0009463
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandUlnar deviation of the 2nd finger (HP:0009464) help
..expandUlnar deviation of the 4th finger (HP:0009278) help
..expandUlnar deviation of the 5th finger (HP:0009180) help
..expandUlnar deviation of thumb (HP:0006156) 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:0009463HP:0009463Ulnar deviation of the 3rd finger0GDF5 CL E G H82004220OMIM:113100Brachydactyly, type CHP:0040282 - Frequent52
HP:0009463HP:0009463Ulnar deviation of the 3rd finger0PTRH2 CL E G H5165124265ORPHA:456312Infantile multisystem neurologic-endocrine-pancreatic diseaseHP:0040283 - Occasional6


Genes (2) :GDF5 PTRH2

Diseases (2) :OMIM:113100 ORPHA:456312
 

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