Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the middle phalanx of the 5th finger (HP:0004219)help
Grandparent Node:
expandSymphalangism of middle phalanx of finger (HP:0009849)help
Grandparent Node:
expandSymphalangism of the 5th finger (HP:0004218)help
Parent Node:
expandAbnormality of the distal phalanx of the 5th finger (HP:0004225)help
Parent Node:
expandDistal symphalangism of hands (HP:0001204)help
Parent Node:
expandSymphalangism of middle phalanx of 5th finger (HP:0009178)help
..Starting node
..expandDistal/middle symphalangism of 5th finger (HP:0009244)help
Term ID: 9244
Name: Distal/middle symphalangism of 5th finger
Synonym: Fifth finger distal interphalangeal joint symphalangism; Fused end and middle bones of little finger; Fused end and middle bones of pinkie finger; Fused end and middle bones of pinky finger; Fusion of the terminal and middle phalanges of the 5th finger; Symphalangism of the distal and middle phalanges of the 5th finger; Symphalangism of the terminal and middle phalanges of the 5th finger
Definition: Fusion of the terminal/distal and middle phalanges of the 5th finger.
Comments:
Reference: HP:0009244
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProximal/middle symphalangism of 5th finger (HP:0009177) 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:0009244HP:0009244Distal/middle symphalangism of 5th finger0TFAP2B CL E G H702111743OMIM:169100Char syndrome.104


Genes (1) :TFAP2B

Diseases (1) :OMIM:169100
 

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