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:
Abnormality of upper limb epiphysis morphology (HP:0003839)

Parent Node:
Abnormality of the humeral epiphyseal plate (HP:0003905)

Parent Node:
Wide epiphyseal plates of the upper limbs (HP:0003846)

..Starting node
..Broad humeral epiphyseal plate (HP:0003906)

Term ID:

3906

Name:

Broad humeral epiphyseal plate

Synonym:

Wide humeral epiphyseal plate; Wide long bone of arm growth plate

Definition:

Increased width of the humeral epiphyseal growth plate.

Comments:

Reference:

HP:0003906

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003906	HP:0003906	Broad humeral epiphyseal plate	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.