Human Phenotype Ontology 
Grandparent Node:
expandAbnormal finger phalanx morphology (HP:0005918)help
Parent Node:
expandFinger hyperphalangy (HP:0030367)help
..Starting node
..expandHyperphalangy of the 2nd finger (HP:0030368)help
Term ID: 30368
Name: Hyperphalangy of the 2nd finger
Synonym: Hyperphalangy of index finger
Definition: An accessory phalanx of the index (second) finger that is arranged linearly with the other phalanges. Hyperphalangy of the index finger results from an accessory ossification center at the metacarpophalangeal joint, resulting in radial deviation of the index finger. Note that this term refers only to this type of hyperphalangy.
Comments:
Reference: HP:0030368
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHyperphalangy of the 3rd finger (HP:0031010) 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:0030368HP:0030368Hyperphalangy of the 2nd finger0TGDS CL E G H2348320324OMIM:616145Catel-Manzke syndrome.6


Genes (1) :TGDS

Diseases (1) :OMIM:616145
 

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