Human Phenotype Ontology 
Grandparent Node:
expandAbnormal finger phalanx morphology (HP:0005918)help
Grandparent Node:
expandOsteolytic defects of the hand bones (HP:0009699)help
Parent Node:
expandAbnormal proximal phalanx morphology of the hand (HP:0009834)help
Parent Node:
expandOsteolytic defects of the phalanges of the hand (HP:0009771)help
..Starting node
..expandOsteolytic defects of the proximal phalanges of the hand (HP:0009855)help
Term ID: 9855
Name: Osteolytic defects of the proximal phalanges of the hand
Synonym: Proximal phalanges osteolysis
Definition:
Comments:
Reference: HP:0009855
Genes and Diseases:
 
       Child Nodes:
........expandOsteolytic defects of the proximal phalanx of the 5th finger (HP:0009230) help
........expandOsteolytic defects of the proximal phalanx of the 4th finger (HP:0009312) help
........expandOsteolytic defects of the proximal phalanx of the 3rd finger (HP:0009453) help
........expandOsteolytic defects of the proximal phalanx of the 2nd finger (HP:0009584) help

 Sister Nodes: 
..expandOsteolytic defect of thumb phalanx (HP:0009654) help
..expandOsteolytic defects of the distal phalanges of the hand (HP:0009839) help
..expandOsteolytic defects of the middle phalanges of the hand (HP:0009847) help
..expandOsteolytic defects of the phalanges of the 2nd finger (HP:0009550) help
..expandOsteolytic defects of the phalanges of the 3rd finger (HP:0009443) help
..expandOsteolytic defects of the phalanges of the 4th finger (HP:0004195) help
..expandOsteolytic defects of the phalanges of the 5th finger (HP:0004216) 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:0009855HP:0009855Osteolytic defects of the proximal phalanges of the hand0 CL E G H
HP:0009855HP:0009584Osteolytic defects of the proximal phalanx of the 2nd finger1 CL E G H
HP:0009855HP:0009453Osteolytic defects of the proximal phalanx of the 3rd finger1 CL E G H
HP:0009855HP:0009312Osteolytic defects of the proximal phalanx of the 4th finger1 CL E G H
HP:0009855HP:0009230Osteolytic defects of the proximal phalanx of the 5th 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.