Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal musculoskeletal physiology (HP:0011843)help
Grandparent Node:
expand
Increased inflammatory response (HP:0012649)help
Parent Node:
expand
Osteomyelitis (HP:0002754)help
..Starting node
..expand
Salmonella osteomyelitis (HP:0005661)help
Term ID: 5661
Name: Salmonella osteomyelitis
Synonym: Salmonella bone infection
Definition: Osteomyelitis caused by infection with the bacteria, salmonella.
Comments:
Reference: HP:0005661
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFoot osteomyelitis (HP:0001886) help
..expandMandibular osteomyelitis (HP:0007626) help
..expandobsolete Chronic recurrent multifocal osteomyelitis (HP:0005901) help
..expandOsteomyelitis leading to amputation due to slow healing fractures (HP:0005010) 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:0005661HP:0005661Salmonella osteomyelitis0IFNGR1 CL E G H34595439OMIM:209950Immunodeficiency 27A, mycobacteriosis, AR.60
HP:0005661HP:0005661Salmonella osteomyelitis0IFNGR1 CL E G H34595439OMIM:615978Immunodeficiency 27B.60
HP:0005661HP:0005661Salmonella osteomyelitis0IL12RB1 CL E G H35945971ORPHA:319552Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiencyHP:0040283 - Occasional46


Genes (2) :IFNGR1 IL12RB1

Diseases (3) :OMIM:209950 OMIM:615978 ORPHA:319552
 

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