Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the phalanges of the 2nd finger (HP:0009541)help
Grandparent Node:
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Broad phalanges of the hand (HP:0009768)help
Parent Node:
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Abnormality of the middle phalanx of the 2nd finger (HP:0009543)help
Parent Node:
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Broad middle phalanx of finger (HP:0009844)help
Parent Node:
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Broad phalanges of the 2nd finger (HP:0009547)help
..Starting node
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Broad middle phalanx of the 2nd finger (HP:0009569)help
Term ID: 9569
Name: Broad middle phalanx of the 2nd finger
Synonym: Broad middle bone of the index finger
Definition: Increased width of the middle phalanx of the second finger.
Comments:
Reference: HP:0009569
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBroad distal phalanx of the 2nd finger (HP:0009558) help
..expandBroad proximal phalanx of the 2nd finger (HP:0009581) 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:0009569HP:0009569Broad middle phalanx of the 2nd finger0 CL E G H


Genes (0) :

Diseases (0) :
 

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