Human Phenotype Ontology 
Grandparent Node:
expandAbnormal skeletal morphology (HP:0011842)help
Parent Node:
expandAbnormal joint morphology (HP:0001367)help
..Starting node
..expandProgressive joint destruction (HP:0005187)help
Term ID: 5187
Name: Progressive joint destruction
Synonym:
Definition:
Comments:
Reference: HP:0005187
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal sacroiliac joint morphology (HP:0100781) help
..expandAbnormality of joint mobility (HP:0011729) help
..expandAbnormality of lower limb joint (HP:0100491) help
..expandAbnormality of the synovia (HP:0005262) help
..expandAbnormality of upper limb joint (HP:0009810) help
..expandArthritis (HP:0001369) help
..expandArthropathy (HP:0003040) help
..expandChondrocalcinosis (HP:0000934) help
..expandEnlarged joints (HP:0003037) help
..expandJoint dislocation (HP:0001373) help
..expandJoint hemorrhage (HP:0005261) help
..expandJoint swelling (HP:0001386) help
..expandOsteochondrosis (HP:0040188) help
..expandPterygium (HP:0001059) 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:0005187HP:0005187Progressive joint destruction0F8 CL E G H21573546ORPHA:169802Severe hemophilia AHP:0040283 - Occasional303


Genes (1) :F8

Diseases (1) :ORPHA:169802
 

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