Human Phenotype Ontology 
Grandparent Node:
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Abnormal 4th finger phalanx morphology (HP:0009172)help
Grandparent Node:
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Finger symphalangism (HP:0009700)help
Grandparent Node:
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Symphalangism affecting the phalanges of the hand (HP:0009773)help
Parent Node:
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Abnormality of the proximal phalanx of the 4th finger (HP:0009284)help
Parent Node:
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Symphalangism affecting the proximal phalanges of the hand (HP:0009857)help
Parent Node:
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Symphalangism of the 4th finger (HP:0004197)help
..Starting node
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Symphalangism affecting the proximal phalanx of the 4th finger (HP:0009314)help
Term ID: 9314
Name: Symphalangism affecting the proximal phalanx of the 4th finger
Synonym: Fused innermost bone of ring finger
Definition: Fusion of the proximal phalanx of the 4th finger with another bone.
Comments:
Reference: HP:0009314
Genes and Diseases:
 
       Child Nodes:
........expandProximal/middle symphalangism of 4th finger (HP:0009477) help
........expandSymphalangism of the proximal phalanx of the 4th finger with the 4th metatcarpal (HP:0009478) help

 Sister Nodes: 
..expandSymphalangism of middle phalanx of 4th finger (HP:0009308) 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:0009314HP:0009314Symphalangism affecting the proximal phalanx of the 4th finger0NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122
HP:0009314HP:0009478Symphalangism of the proximal phalanx of the 4th finger with the 4th metacarpal1 CL E G H
HP:0009314HP:0009477Proximal/middle symphalangism of 4th finger1NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122


Genes (1) :NOG

Diseases (1) :OMIM:186500
 

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