Human Phenotype Ontology 
Grandparent Node:
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Aplasia/Hypoplasia of the proximal phalanges of the hand (HP:0009851)help
Grandparent Node:
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Short finger (HP:0009381)help
Grandparent Node:
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Short phalanx of finger (HP:0009803)help
Parent Node:
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Aplasia/Hypoplasia of the proximal phalanx of the 5th finger (HP:0009192)help
Parent Node:
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Short 5th finger (HP:0009237)help
Parent Node:
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Short proximal phalanx of finger (HP:0010241)help
..Starting node
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Short proximal phalanx of the 5th finger (HP:0009226)help
Term ID: 9226
Name: Short proximal phalanx of the 5th finger
Synonym: Hypoplastic/small proximal phalanx of the 5th finger; Short innermost little finger bone; Short innermost pinkie finger bone; Short innermost pinky finger bone; Short proximal phalanx of the fifth finger
Definition: Hypoplastic/small proximal phalanx of the fifth finger.
Comments:
Reference: HP:0009226
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandShort proximal phalanx of the 2nd finger (HP:0009597) help
..expandShort proximal phalanx of the 3rd finger (HP:0009459) help
..expandShort proximal phalanx of the 4th finger (HP:0009301) help
..expandShortening of all proximal phalanges of the fingers (HP:0006144) 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:0009226HP:0009226Short proximal phalanx of the 5th finger0KIF15 CL E G H5699217273ORPHA:26132321q22.11q22.12 microdeletion syndromeHP:0040283 - Occasional


Genes (1) :KIF15

Diseases (1) :ORPHA:261323
 

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