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 morphology of phalanx of the 2nd toe (HP:0010324)

Grandparent Node:
Broad phalanx of the toes (HP:0010174)

Parent Node:
Abnormality of the middle phalanx of the 2nd toe (HP:0010357)

Parent Node:
Broad middle phalanges of the toes (HP:0010195)

Parent Node:
Broad phalanges of the 2nd toe (HP:0010348)

..Starting node
..Broad middle phalanx of the 2nd toe (HP:0010405)

Term ID:

10405

Name:

Broad middle phalanx of the 2nd toe

Synonym:

Broad middle bone of 2nd toe

Definition:

Comments:

Reference:

HP:0010405

Genes and Diseases:

Child Nodes:

Sister Nodes:

Broad distal phalanx of the 2nd toe (HP:0010414)

Broad proximal phalanx of the 2nd toe (HP:0010396)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010405	HP:0010405	Broad middle phalanx of the 2nd toe	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.