Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 lower-limb metaphysis morphology (HP:0006490)

Grandparent Node:
Abnormality of tibia morphology (HP:0002992)

Parent Node:
Abnormal tibial metaphysis morphology (HP:0006491)

..Starting node
..Broad tibial metaphyses (HP:0006413)

Term ID:

6413

Name:

Broad tibial metaphyses

Synonym:

Broad wide portion of shankbone; Broad wide portion of shinbone

Definition:

Comments:

Reference:

HP:0006413

Genes and Diseases:

Child Nodes:

Sister Nodes:

Peg-like central prominence of distal tibial metaphyses (HP:0006423)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006413	HP:0006413	Broad tibial metaphyses	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.