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 carpal morphology (HP:0001191)

Parent Node:
Abnormality of carpal bone ossification (HP:0006257)

Parent Node:
Abnormality of the trapezoid bone (HP:0004256)

..Starting node
..Abnormal ossification of the trapezoid bone (HP:0045004)

Term ID:

45004

Name:

Abnormal ossification of the trapezoid bone

Synonym:

Definition:

Comments:

Reference:

HP:0045004

Genes and Diseases:

Child Nodes:

........

Delayed ossification of the trapezoid bone (HP:0004257)

Sister Nodes:

Absent trapezoid bone (HP:0006106)

Small trapezoid bone (HP:0004258)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0045004	HP:0045004	Abnormal ossification of the trapezoid bone	0	CL E G H
HP:0045004	HP:0004257	Delayed ossification of the trapezoid bone	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.