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 long bone morphology (HP:0011314)

Grandparent Node:
Abnormal morphology of the radius (HP:0002818)

Grandparent Node:
Obsolete Abnormal forearm bone morphology (HP:0040073)

Parent Node:
Broad forearm bones (HP:0003971)

Parent Node:
Broad long bones (HP:0005622)

Parent Node:
obsolete Abnormal morphology of the radius (HP:0045009)

..Starting node
..Broad radius (HP:0003981)

Term ID:

3981

Name:

Broad radius

Synonym:

Wide radius

Definition:

Increased width of the radius.

Comments:

Reference:

HP:0003981

Genes and Diseases:

Child Nodes:

........

Broad radial metaphysis (HP:0004026)

Sister Nodes:

Abnormal shape of the radius (HP:0045008)

Constricted radius (HP:0003976)

Deformed radius (HP:0003977)

Elongated radius (HP:0006424)

Fractured radius (HP:0003978)

Hypoplasia of the radius (HP:0002984)

Radial dysplasia (HP:0006433)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003981	HP:0003981	Broad radius	0	CL E G H
HP:0003981	HP:0004026	Broad radial metaphysis	1	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.