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:
Polydactyly (HP:0010442)

Parent Node:
Hand polydactyly (HP:0001161)

Parent Node:
Mirror image polydactyly (HP:0010689)

..Starting node
..Mirror image hand polydactyly (HP:0010690)

Term ID:

10690

Name:

Mirror image hand polydactyly

Synonym:

Mirror image dupliction of fingers

Definition:

Mirror image duplication of digits affecting the hands only.

Comments:

Reference:

HP:0010690

Genes and Diseases:

Child Nodes:

Sister Nodes:

Mirror image foot polydactyly (HP:0010691)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010690	HP:0010690	Mirror image hand polydactyly	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.