Human Phenotype Ontology 
Grandparent Node:
expandAbnormal appendicular skeleton morphology (HP:0011844)help
Grandparent Node:
expandAbnormality of limb bone (HP:0040068)help
Parent Node:
expandAbnormality of limb bone morphology (HP:0002813)help
..Starting node
..expandLimb duplication (HP:0100524)help
Term ID: 100524
Name: Limb duplication
Synonym: Dimelia; Limb duplication
Definition: Congenital duplication of all or part of a limb.
Comments:
Reference: HP:0100524
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal digit morphology (HP:0011297) help
..expandAbnormal limb epiphysis morphology (HP:0006505) help
..expandAbnormal metaphysis morphology (HP:0000944) help
..expandAbnormal radial ray morphology (HP:0410049) help
..expandAbsent ray (HP:0030030) help
..expandAcromicria (HP:0031878) help
..expandAplasia/hypoplasia involving bones of the extremities (HP:0045060) help
..expandEctrodactyly (HP:0100257) help
..expandobsolete Abnormal morphology of bones of the lower limbs (HP:0040066) help
..expandobsolete Abnormal morphology of bones of the upper limbs (HP:0040065) help
..expandobsolete Anomaly of the limb diaphyses morphology (HP:0006504) help
..expandSubperiosteal bone resorption (HP:0003106) 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:0100524HP:0100524Limb duplication0LMBR1 CL E G H6432713243ORPHA:2378Laurin-Sandrow syndromeHP:0040282 - Frequent106


Genes (1) :LMBR1

Diseases (1) :ORPHA:2378
 

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