Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal musculoskeletal physiology (HP:0011843)

Grandparent Node:
Increased inflammatory response (HP:0012649)

Parent Node:
Osteomyelitis (HP:0002754)

..Starting node
..obsolete Chronic recurrent multifocal osteomyelitis (HP:0005901)

Term ID:

5901

Name:

obsolete Chronic recurrent multifocal osteomyelitis

Synonym:

Definition:

Comments:

Reference:

HP:0005901

Genes and Diseases:

Child Nodes:

Sister Nodes:

Foot osteomyelitis (HP:0001886)

Mandibular osteomyelitis (HP:0007626)

Osteomyelitis leading to amputation due to slow healing fractures (HP:0005010)

Salmonella osteomyelitis (HP:0005661)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005901	HP:0005901	obsolete Chronic recurrent multifocal osteomyelitis	0	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.