Human Phenotype Ontology 
Grandparent Node:
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Abnormal skeletal muscle morphology (HP:0011805)help
Parent Node:
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Myopathy (HP:0003198)help
..Starting node
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Inflammatory myopathy (HP:0009071)help
Term ID: 9071
Name: Inflammatory myopathy
Synonym:
Definition: Chronic muscle inflammation accompanied by muscle weakness.
Comments:
Reference: HP:0009071
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEMG: myopathic abnormalities (HP:0003458) help
..expandMinicore myopathy (HP:0003789) help
..expandMyofibrillar myopathy (HP:0003715) help
..expandNecrotizing myopathy (HP:0008978) help
..expandSkeletal myopathy (HP:0003756) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0009071HP:0009071Inflammatory myopathy0CAV3 CL E G H859123320Elevated serum creatine phosphokinase123320C0241005OMIM14171529601253
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :CAV3

Diseases (1) :123320
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.