Human Phenotype Ontology 
Grandparent Node:
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Abnormal epiphysis morphology of the phalanges of the hand (HP:0005920)help
Grandparent Node:
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Absent epiphyses (HP:0010577)help
Parent Node:
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Abnormality of the epiphyses of the 4th finger (HP:0009174)help
Parent Node:
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Absent epiphyses of the phalanges of the hand (HP:0010228)help
..Starting node
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Absent epiphyses of the 4th finger (HP:0009393)help
Term ID: 9393
Name: Absent epiphyses of the 4th finger
Synonym: Absent end part of the ring finger bone
Definition: Absence of one or more epiphyses of the 4th finger.
Comments:
Reference: HP:0009393
Genes and Diseases:
 
       Child Nodes:
........expandAbsent epiphysis of the middle phalanx of the 4th finger (HP:0009214) help
........expandAbsent epiphysis of the distal phalanx of the 4th finger (HP:0009250) help
........expandAbsent epiphysis of the proximal phalanx of the 4th finger (HP:0009261) help

 Sister Nodes: 
..expandAbsent epiphyses of the 2nd finger (HP:0009488) help
..expandAbsent epiphyses of the 3rd finger (HP:0009410) help
..expandAbsent epiphyses of the 5th finger (HP:0009382) help
..expandAbsent epiphyses of the distal phalanges of the hand (HP:0010246) help
..expandAbsent epiphyses of the middle phalanges of the hand (HP:0010257) help
..expandAbsent epiphyses of the proximal phalanges of the hand (HP:0010268) help
..expandAbsent epiphyses of the thumb (HP:0009686) 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:0009393HP:0009393Absent epiphyses of the 4th finger0 CL E G H
HP:0009393HP:0009261Absent epiphysis of the proximal phalanx of the 4th finger1 CL E G H
HP:0009393HP:0009250Absent epiphysis of the distal phalanx of the 4th finger1 CL E G H
HP:0009393HP:0009214Absent epiphysis of the middle phalanx of the 4th finger1 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.