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 cortical bone morphology (HP:0003103)

Parent Node:
Abnormality of foot cortical bone (HP:0025332)

..Starting node
..Cortical thinning of foot bones (HP:0025333)

Term ID:

25333

Name:

Cortical thinning of foot bones

Synonym:

Definition:

A reduction in the thickness of the outer shell (cortex) of foot bones.

Comments:

Reference:

HP:0025333

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:0025333	HP:0025333	Cortical thinning of foot bones	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.