Human Phenotype Ontology

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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:
Foot polydactyly (HP:0001829)

Grandparent Node:
Mesoaxial polydactyly (HP:0100260)

Parent Node:
Abnormality of the 2nd toe (HP:0010319)

Parent Node:
Mesoaxial foot polydactyly (HP:0010112)

..Starting node
..Polydactyly affecting the 2nd toe (HP:0010328)

Term ID:

10328

Name:

Polydactyly affecting the 2nd toe

Synonym:

Definition:

Comments:

Reference:

HP:0010328

Genes and Diseases:

Child Nodes:

Sister Nodes:

Polydactyly affecting the 3rd toe (HP:0010334)

Polydactyly affecting the 4th toe (HP:0010340)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010328	HP:0010328	Polydactyly affecting 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.