Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the dentition (HP:0000164)help
Parent Node:
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Abnormality of dental morphology (HP:0006482)help
..Starting node
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Double tooth (HP:0011089)help
Term ID: 11089
Name: Double tooth
Synonym: Conjoined teeth; Double tooth; Teeth, double; Twinning tooth
Definition: Fusion of two adjacent teeth.
Comments:
Reference: HP:0011089
Genes and Diseases:
 
       Child Nodes:
........expandFused teeth (HP:0011090) help
........expandGemination (HP:0011091) help

 Sister Nodes: 
..expandAbnormal dental root morphology (HP:0006486) help
..expandAbnormal incisor morphology (HP:0011063) help
..expandAbnormal molar morphology (HP:0011070) help
..expandAbnormal premolar morphology (HP:0011080) help
..expandConical tooth (HP:0000698) help
..expandMacrodontia (HP:0001572) help
..expandMicrodontia (HP:0000691) 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:0011089HP:0011089Double tooth0BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2101
HP:0011089HP:0011089Double tooth0BCOR CL E G H5488020893ORPHA:2712Oculofaciocardiodental syndrome101
HP:0011089HP:0011089Double tooth0MED12 CL E G H996811957ORPHA:93932FG syndrome type 1228
HP:0011089HP:0011089Double tooth0SLC35A2 CL E G H735511022OMIM:300896Congenital disorder of glycosylation, type IIm27
HP:0011089HP:0011089Double tooth0WDR35 CL E G H5753929250OMIM:613610Cranioectodermal dysplasia 2136
HP:0011089HP:0011089Double tooth0WDR35 CL E G H5753929250OMIM:614091Short-Rib thoracic dysplasia 7 with or without polydactyly136
HP:0011089HP:0011091Gemination1 CL E G H
HP:0011089HP:0011090Fused teeth1BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2.101
HP:0011089HP:0011090Fused teeth1BCOR CL E G H5488020893ORPHA:2712Oculofaciocardiodental syndromeHP:0040282 - Frequent101
HP:0011089HP:0011090Fused teeth1MED12 CL E G H996811957ORPHA:93932FG syndrome type 1HP:0040282 - Frequent228
HP:0011089HP:0011090Fused teeth1SLC35A2 CL E G H735511022OMIM:300896Congenital disorder of glycosylation, type IIm27
HP:0011089HP:0011090Fused teeth1WDR35 CL E G H5753929250OMIM:613610Cranioectodermal dysplasia 2136
HP:0011089HP:0011090Fused teeth1WDR35 CL E G H5753929250OMIM:614091Short-Rib thoracic dysplasia 7 with or without polydactyly.136


Genes (4) :BCOR MED12 SLC35A2 WDR35

Diseases (6) :OMIM:300166 ORPHA:2712 ORPHA:93932 OMIM:300896 OMIM:613610 OMIM:614091
 

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