Human Phenotype Ontology 
Grandparent Node:
expandAbnormal ear morphology (HP:0031703)help
Parent Node:
expandAbnormality of the middle ear (HP:0000370)help
Parent Node:
expandAbnormality of the outer ear (HP:0000356)help
..Starting node
..expandAbnormality of the tympanic membrane (HP:0040090)help
Term ID: 40090
Name: Abnormality of the tympanic membrane
Synonym: Abnormality of the eardrum
Definition: An abnormality of the tympanic membrane
Comments:
Reference: HP:0040090
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
..expandAplasia/Hypoplasia of the external ear (HP:0008772) help
..expandExternal ear malformation (HP:0008572) help
..expandExtra concha fold (HP:0400002) help
..expandHypertrophic auricular cartilage (HP:0008608) 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:0040090HP:0040090Abnormality of the tympanic membrane0 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.