Human Phenotype Ontology 
Grandparent Node:
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Abnormal musculoskeletal physiology (HP:0011843)help
Grandparent Node:
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Increased inflammatory response (HP:0012649)help
Parent Node:
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Abnormal mandible morphology (HP:0000277)help
Parent Node:
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Osteomyelitis (HP:0002754)help
..Starting node
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Mandibular osteomyelitis (HP:0007626)help
Term ID: 7626
Name: Mandibular osteomyelitis
Synonym: Lower jaw bone infection; Osteomyelitis, especially of the mandible
Definition: Osteomyelitis of the lower jaw.
Comments:
Reference: HP:0007626
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFoot osteomyelitis (HP:0001886) help
..expandobsolete Chronic recurrent multifocal osteomyelitis (HP:0005901) help
..expandOsteomyelitis leading to amputation due to slow healing fractures (HP:0005010) help
..expandSalmonella osteomyelitis (HP:0005661) 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:0007626HP:0007626Mandibular osteomyelitis0ANO5 CL E G H20385927337ORPHA:53697Gnathodiaphyseal dysplasiaHP:0040282 - Frequent304
HP:0007626HP:0007626Mandibular osteomyelitis0CLCN7 CL E G H11862025ORPHA:53Albers-Schönberg osteopetrosisHP:0040281 - Very frequent102
HP:0007626HP:0007626Mandibular osteomyelitis0CLCN7 CL E G H11862025OMIM:166600Osteopetrosis, autosomal dominant 2.102
HP:0007626HP:0007626Mandibular osteomyelitis0TNFSF11 CL E G H860011926OMIM:259710Osteopetrosis, autosomal recessive 2.44


Genes (3) :ANO5 CLCN7 TNFSF11

Diseases (4) :ORPHA:53697 ORPHA:53 OMIM:166600 OMIM:259710
 

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