Human Phenotype Ontology 
Grandparent Node:
expandAbnormal ear morphology (HP:0031703)help
Parent Node:
expandAbnormality of the outer ear (HP:0000356)help
..Starting node
..expandHypertrophic auricular cartilage (HP:0008608)help
Term ID: 8608
Name: Hypertrophic auricular cartilage
Synonym:
Definition:
Comments:
Reference: HP:0008608
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal location of ears (HP:0000357) help
..expandAbnormal pinna morphology (HP:0000377) help
..expandAbnormality of cartilage of external ear (HP:3000022) help
..expandAbnormality of the auditory canal (HP:0000372) help
..expandAbnormality of the tympanic membrane (HP:0040090) help
..expandAplasia/Hypoplasia of the external ear (HP:0008772) help
..expandExternal ear malformation (HP:0008572) help
..expandExtra concha fold (HP:0400002) help
..expandNeoplasm of the outer ear (HP:0040095) help
..expandobsolete Bilateral external ear deformity (HP:0040111) help
..expandPolyotia (HP:0100687) help
..expandTelangiectasia of the ear (HP:0009893) help
..expandUnilateral external ear deformity (HP:0008605) 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:0008608HP:0008608Hypertrophic auricular cartilage0SLC26A2 CL E G H183610994OMIM:222600Diastrophic dysplasia.166


Genes (1) :SLC26A2

Diseases (1) :OMIM:222600
 

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