Human Phenotype Ontology 
Grandparent Node:
expandAbnormal digit morphology (HP:0011297)help
Parent Node:
expandPolydactyly (HP:0010442)help
..Starting node
..expandMirror image polydactyly (HP:0010689)help
Term ID: 10689
Name: Mirror image polydactyly
Synonym: Mirror image duplication of digits
Definition: A hand or foot with more than five digits that has a recognizable A/P axis of symmetry. The axis can lie within a normally formed or partially duplicated digit resembling a middle finger, index finger, thumb, toe, or hallux. Alternatively, the axis can be in an interdigital space with a flanking pair of digits that resemble a middle finger, index finger, thumb, toe or hallux. The most lateral digits on each side of the hand/foot typically resemble fifth fingers/toes.
Comments:
Reference: HP:0010689
Genes and Diseases:
 
       Child Nodes:
........expandMirror image hand polydactyly (HP:0010690) help
........expandMirror image foot polydactyly (HP:0010691) help

 Sister Nodes: 
..expandFoot polydactyly (HP:0001829) help
..expandHand polydactyly (HP:0001161) help
..expandMesoaxial polydactyly (HP:0100260) help
..expandPostaxial polydactyly (HP:0100259) help
..expandPreaxial polydactyly (HP:0100258) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010689HP:0010689Mirror image polydactyly0LMBR1 CL E G H6432713243ORPHA:2378Laurin-Sandrow syndromeHP:0040281 - Very frequent106
HP:0010689HP:0010689Mirror image polydactyly0PITX1 CL E G H53079004OMIM:119800CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY; CCF8
HP:0010689HP:0010690Mirror image hand polydactyly1 CL E G H
HP:0010689HP:0010691Mirror image foot polydactyly1PITX1 CL E G H53079004OMIM:119800CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY; CCF8


Genes (2) :LMBR1 PITX1

Diseases (2) :ORPHA:2378 OMIM:119800
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.